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User guide
G and C
The Axiom range is the result of close collaboration between a panel of expert
Success for you means success for us. Our marketing network and team of
experts is always available to you for any further information that you may
need.
> Scope
The Axiom system is exclusively intended to replace missing teeth. It enables one or more
artificial roots to be positioned, onto which dental prostheses are fixed and/ or stabilised.
The system allows single-unit, multiple-unit or complete restoration to be performed.
TRAINING:
Axiom components should only be implanted by practitioners who have been trained in implant practice and/or prosthetic techniques, and who are equipped for this type of procedure. Correct knowledge of surgical techniques and prosthetics is required to use
this system.
Specific training is offered and delivered at the Anthogyr company.
The surgical and prosthetic technique for the Axiom system is performed exclusively in conjunction with the original components and
instruments in accordance with the manufacturers recommendations. Anthogyr can take no responsibility in case of placement noncompliant with this manual and in case of use of implants or prosthetic parts or instruments foreign to the system.
Clinical evaluation of the patient and the choice of treatment solution are the sole responsibility of the practitioner. The implant
diameter and length must be determined beforehand by the dental practitioner, depending on the clinical situation. Patients should
also be informed of potential risks associated with implanting this type of device : oedema, bruising, haemorrhage, periodontal complications, transient or permanent nerve damage, local or systemic infections or inflammation, bone fractures, loosening or fracture
of the implant, dehiscence, aesthetic problems, aspirating or swallowing the device, iatrogenic trauma etc.
EQUIPMENT:
The practitioner using the system is responsible for the follow-up and maintenance procedures required to identify and treat any
complications as early as possible and for ensuring the correct functioning and safety of the device. The references and the batch
numbers of all components implanted, temporarily and/or definitively, must be recorded in the medical file of the patient. Follow-up
and maintenance are part of the knowledge of a practitioner trained in placing dental implants.
The practitioner is also responsible for defining the different settings for his/her equipment (instrument rotation speed, irrigation
flow rate, etc), according to each clinical case, and for confirming that these are in good condition before each procedure.
Reusable instruments must be cleaned, decontaminated and sterilised before each surgery (even when first used) in accordance
with current protocols in hospitals and clinics. The organisation of the operating room, preparation of operating staff and of the patient (premedication, anaesthesia, etc) should follow current procedures and are the responsibility of the practitioner.
Anthogyr can under no circumstances be held responsible for any harm arising from defective handling or use.
In order to avoid swallowing or inhaling small components, it is recommended that these are rendered secure by fixing them to the
outside of the mouth with a suture thread. Whenever an instrument is changed, confirm that the contra-angle or key are correctly
fixed by applying slight traction and ensure that each part is correctly fixed onto the transfer system outside the oral cavity.
CONSERVATION :
In producing our products, we have paid particular care and guarantee that a manufacturing control has been performed on all
products made available for sale. In order to guarantee their integrity, it is recommended that they be stored in their original
packaging at an ambient temperature of between 15 and 30C, away from moisture and direct sunlight.
Protect packages from dust and do not store in the same premises as solvents and/or paints containing solvents or chemical
substances.
The device must be used before the expiration date indicated on the traceability label.
If the package (blister-closure / bag) is damaged or a defect is apparent when the product is opened, it is imperative that the
device not be used and that the nature of the defect, part numbers and batch numbers of the components concerned are reported to the distributor or to Anthogyr.
The technical specifications contained within these instructions are provided for indicative purposes only and cannot form the
subject of any complaint.
The Axiom implant system must not be used on animals.
Single-use devices must not be reused, nor resterilised (risk of contamination and risk of alteration of functional surfaces).
The instructions for use here in may only be reproduced or disseminated with prior approval from the Anthogyr company. Anthogyr reserves the right to vary the technical feature of its products and/or to make changes or improvements to the Axiom
system without prior notice.
The Axiom implant system is not compatible with other Anthogyr and competitors systems.
If uncertain, the user should contact the Anthogyr company before use.
This manual cancels and replaces all previous versions.
TABLE OF CONTENTS
1. Axiom, the new dimension
2. Surgical Protocols
12
E/ OSTEOTOMY PROTOCOLS
15
16
20
21
22
24
3. Prosthetic protocols
A/ CONSTANT EMERGENCE PROFILE OF THE AXIOM RANGE
29
29
30
32
33
35
37
39
41
43
45
46
62
68
71
72
73
A/ GENERAL INFO
73
B/ PRODUCTS
74
C/ PROTOCOLS
75
5. Disassembling Re-assembly
77
76
B/ INSTRUMENT KIT
77
78
78
78
79
79
B/ SURGICAL INSTRUMENTS
81
C/ PROSTHETIC COMPONENTS
86
D/ REWORKING KIT
103
S
O
N
B
V
E
F
g
Device sterilised by
Gamma irradiation
Manufacturing batch
number of the device
Commercial part number
of the device
Manufacturing date
of the device
Expiration date of
the device
W
Y
X
Z
k
A
Do not sterilise
by autoclaving
Do not re-use,
single use device
Protect from light
Do not use
if packaging is damaged
Keep dry
30C
15C
Warning : observe
instructions for use
Non-sterile device
G/K
Temperature restrictions
Manufacturer
Class I or Class IIa/IIb medical device
complying with European Directive 93/42/EEC
Tightening torque
2. Surgical Protocols
A. AXIOM REG AND AXIOM PX RANGE OF IMPLANTS
The Axiom implant system has been designed in order to enhance the functional and aesthetic integration of implant
supported restorations.
BONE DENSITY
IMPLANTS
Axiom REG
Axiom PX
D1
D2-D3
D4
OK
OK
OK
NOT RECOMMENDED
OK
OK
2. Axiom REG and Axiom PX implants are made of Grade V Medical Titanium, high-resistance biocompatible material (in
compliance with US standard ASTM F136 and international ISO 5832-3 standard). They benefit from a BCP osseo-conductive
surface treatment (surface treatment with BCP sand-blasting).
SINGLE CONNECTION
2.7
3.4
4.0
4.6
5.2
3.4
SIMPLICITY
One connection, common for
the implants Axiom REG and
Axiom PX
4.0
4.6
5.2
Gauges
Mandrel extension
Mandrel key
Drill guide
S drills*
Round bur
Pointer drill
Reversible ratchet
wrench
DRILLING
Initial drill 2.0 mm
Lindemann bur
1 500 rpm
TAPPING
Optional (D1 Bone)(2)
20-25 rpm
DRILLING
Drilling sequences
1 000 rpm
(1)
TIGHTENING
Placing the implant
25 rpm
TWO-STAGE SURGERY
1. Positioning the
cover screw
IMMEDIATE LOADING
5-10 N.cm
5-10 N.cm
or
or
or
2. Positioning the
healing screw
Temporary
5-10 N.cm
Standard
Conical abutment
straight/angulated
Multi-unit abutment
straight/angulated
The implant diameter and length must be determined beforehand by the dental practitioner, depending on the clinical situation.
E 3.4 mm implants are not recommended for single tooth restorations in the molar region.
3.4 mm
3
4.0 mm
4.6 mm
5.2 mm
(1) Optional tool
6,5 mm
6,5 mm
6,5 mm
8 mm
8 mm
8 mm
8 mm
10 mm
10 mm
10 mm
10 mm
12 mm
12 mm
12 mm
12 mm
14 mm
14 mm
14 mm
14 mm
16 mm
16 mm
18 mm
18 mm
IMPLANT CODING:
Sales Reference
Implant Code
OP
34
dd
40
lll
46
52
implant
060
080
100
Implant
120 length
140
160
180
DRILLING DEPTHS:
The Axiom REG placement protocol provides for a subcrestal positioning of the implant .
The surface of the implants shoulder is BCP treated in order to favour peripheral bone healing in this region.
The Axiom REG surgery protocol takes into account an apical overdrilling of 0.5 mm.
WARNING !
The size(s) of the implant(s) shall be pre-defined in the treatment plan. A radiographic template calibrating* film is provided to select
the implant diameter and length according to the bone available.
*The film also takes into consideration the length of the associated drilling.
When selecting the implant, take into consideration the length of the drill +0.5 to 0.6 mm at the tip, added to 0.5 mm in sub-crestal position. These additional lengths are indicated on the calibrating film.
They allow bone chips to be collected during the self-tapping of the implant and they avoid apical over-compression.
Precision of the calibrating film: +/- 2%.
Do not use the calibrating film if it is damaged (poor print quality, tear...).
Drilling
Depth (mm)
DRILLING DEPTH =
LENGTH OF IMPLANT + 1 mm
19.0
17.0
15.0
0.5 mm
13.0
11.0
4.0 x 10mm
9.0
7.5
0.5
0.0
Drill
10
Gauge
Drill
Drill
Tap
optional
Comply with cleaning, decontamination and sterilisation procedures by referring to corresponding section.
Each terminal instrument specific to an Axiom REG implant diameter can be identified by the identification colour code.
The instruments must be used in the chronological order shown below.
All the drills and reamers are available in 2 lengths (S and L). Taps are available in length L.
They have been designed for axial drilling (not transversal drilling), especially drill 2.0 mm.
The 2.0mm Lindemann bur is designed for axial or transverse drilling.
Drills
2.0
2.4 / 3.0
3.0 / 3.6
3.6 / 4.2
4.2 / 4.8
3.4
4.0
4.6
5.2
(2)
Implants
Axiom REG
3.4 mm
Axiom REG
4.0 mm
Axiom REG
4.6 mm
Axiom REG
5.2 mm
Optional tapping.
Recommended for D1-type bone.
x
(2)
Optional tool
11
1. SURGICAL PHASES
Bone overheating should be avoided when drilling, tapping and tightening the implant in order to limit the risk of bone
loss during the osseointegration phase. Bone overheating may be limited using by irrigation or torque control
MARKING
Round bur /Pointer drill
1 500 rpm
DRILLING
Initial drill 2.0 mm
Lindemann bur
1 500 rpm
DRILLING
Drilling sequences
1 000 rpm
(2)
TIGHTENING
Placing the implant
15 rpm
TWO-STAGE SURGERY
1. Positioning the
cover screw
5-10 N.cm
IMMEDIATE LOADING
or
or
Temporary
Standard
Conical abutment
straight/angulated
Multi-unit abutment
straight/angulated
A treatment plan is to be established prior to each implant placement.This plan should include a healing period
which can be re-evaluated during the surgery process if needed.
12
(1) in accordance with C. Mischs classification. [Misch CE, Judy KW (1987), Classification of partially edentulous arches for implant dentistry. Int J Oral
Implants 4(2): 7-13].
(2) Optional tool
implant diameter and length must be determined beforehand by the dental practitioner, depending on the clinical situation.
E The
3.4 mm implants are not recommended for single tooth restorations in the molar region.
3.4 mm
4.0 mm
4.6 mm
5.2 mm
6,5 mm
6,5 mm
8 mm
8 mm
8 mm
8 mm
10 mm
10 mm
10 mm
10 mm
12 mm
12 mm
12 mm
12 mm
14 mm
14 mm
14 mm
14 mm
16 mm
16 mm
18 mm
18 mm
IMPLANT CODING :
Sales Reference
Implant Code
PX
34
dd
40
lll
46
52
implant
060
080
100
120
140
160
180
Implant
length
DRILLING DEPTHS :
The Axiom PX placement protocol provides for a subcrestal positioning of the implant .
The surface of the implants shoulder is BCP treated in order to favour peripheral bone healing in this region.
The Axiom PX surgery protocol takes into account an apical overdrilling of 0.5 mm.
WARNING !
The size(s) of the implant(s) shall be pre-defined in the treatment plan. A radiographic template calibrating film is provided to select to the implant diameter and length according to the bone available.
The film also takes into consideration the length of the associated drilling.
When selecting the implant, take into consideration the length of the drill +0.5 to 0.6 mm at the tip, added to 0.5 mm in
sub-crestal position. The over-drilling is indicated with a triangle on the calibrating film.
They allow bone chips to be collected during the self-tapping of the implant and they avoid apical over-compression.
Precision of the calibrating film : +/- 2%.
Do not use the calibrating film if it is damaged (poor print quality, tear...).
13
Drilling
Depth (mm)
DRILLING DEPTH =
LENGTH OF IMPLANT + 1 mm
19.0
17.0
15.0
0.5 mm
13.0
11.0
4.0 x 10mm
9.0
7.5
0.5
0.0
Drill
Gauge
Drill
cutting instruments (drills, taps, reamers...) are limited to 20 uses and should be used under external irrigation.
(1)
Comply with cleaning, decontamination and sterilisation procedures by referring to corresponding section.
Forets
2.0
2.0 / 2.4
2.4 / 3.0
3.0 / 3.6
3.6 / 4.2
(2)
Implants
Axiom PX
3.4 mm
Axiom PX
4.0 mm
Axiom PX
4.6 mm
Axiom PX
5.2 mm
x
x
WARNING !
Axiom PX implant placement is contraindicated in D1-type bone.
Tapping devices must not be used during the placement of Axiom PX implants
14
Mandrel extension
Osteotomes can be used to prepare the site and implement the Axiom REG/PX implants.
The OSTEO SAFE solution is designed for crestal sinus lifts and/or maxilla bone condensation in low density bone.
D You will also find other information about how to use OSTEO SAFE in the osteotome user guide. (063OSTEOTOMIE_NOT)
15
All implants come with 4 self-sticking, removable, repositionable traceability labels which must be included in the
patient record.
Open the sealed pack without touching the inside of the blister. Carefully
place the tube and cap on a sterile
surface.
16
1 Engage
2 Press
3 Disconnect
1 Press
2 Connect
Withdraw the closure plug by simple traction
3 Release
1 Connect
2 Withdraw
Adjust the speed of the contra-angle.Tighten the implant to the desired depth
Recommended speeds for implant tightening:
Axiom REG : 25 rpm, Axiom PX : 15 rpm
WARNING !
Regulary check the tightening torque in order not to exceed 80 N.cm.
Do not hesitate to unscrew and re-screw during the implants insertion to reduce
screwing forces.
17
MANUAL POSITIONING:
(1)
WARNING !
No tightening torque control. However, it is possible to evaluate the torque using the surgical dynamometric ratchet
wrench Ref. INCCDC. Be careful not apply excessive forces to the connection. Do not hesitate to unscrew and re-screw
during the implants insertion to reduce screwing forces.
WARNING !
Drilling depth = length of implant + 1mm (0.5 mm apical reserve / 0.5 mm below the crest)
3 mm
2 mm
1 mm
0 mm
WARNING !
The implant orientation is a key phase. It pre-determines the final orientation of the prosthetic components.
After osseointegration and bone maturation, the orientation of the prosthesis is irreversible. It is therefore essential to establish the prosthetic treatment plan before surgery, particularly when prosthetic components providing angulation are used.
The implant is finally orientated depending on the desired prosthetic solution and on the component being used.
The tightening wrenches and mandrels have 3 faces, each equipped with a
visual identifier corresponding to the implant indexation.
When screwing or unscrewing the implant, orientate one of the identifier on
the surfaces of the instrument as closely as possible in the appropriate direction depending on the desired prosthetic restoration and situation in the
mouth.
The identifier chosen will define the principal prosthetic orientation of the
components
WARNING !
During angular orientation of the implant by screwing or unscrewing, it is
important to choose the identifier located closest to the final orientation in
order to preserve the apico-coronal positioning.
To adjust (effectively) the implant axis during the prosthetic step, the three-lobe
flat must be placed in the axis of the implants emergence .
NOTE : Sterilisable try-in abutments are available and can be used during the
surgery to check and validate the final positioning of the implant.
19
2. ONE-STAGE SURGERY
It is possible to select the healing screw among 4 emergence profiles in accordance with the size of the tooth/ teeth to be
restored.
Healing screws are supplied Q (single-use).
.
Neck Dia
Mini
Maxi
3.4
4.0
Mandibular incisors
Mes-Dist
2.9
4.1
Mes-Dist
5.5
7.6
Mes-Dist
4.1
5.2
Max. Canine
Mes-Dist
5.3
6.4
Mand. Canine
Mes-Dist
4.5
1 max. molar
Mes-Dist
7.5
Mes-Dist
3.8
5.5
st
Coronary height:
1mm / 2mm
Gingival height:
0.75/1.5/2.5/3.5 and
4.5mm
6.0
5.0
14
12
10
8
6.5
2 Palpate the bottom of the socket (blunt tip) for immediate postextraction implant placement.
3 Check the drilling depth after using the 2.0 mm starter drill (Axiom REG/PX/2.8 implants).
3
2
Drilling
depth (mm)
19.0
17.0
15.0
0.5 mm
13.0
11.0
4.0 x 10mm
9.0
7.5
0.5
0.0
Drill
Gauge
Drill
4.5
2.5
0.75
3.5
1.5
21
IDENTIFY THE DRILL STOP AND UNLOCK KIT FOR ACCESS DRILL STOP :
Unlock
The S stops are identified by a circumferential groove; they are only mounted on S drills.
The L stops are only mounted on L drills.
Circumferential groove
22
4.2 / 4.8mm
3.6 / 4.2mm
3.0 / 3.6mm
2.4 / 3.0mm
2.0 / 2.4mm
2.0mm
Fraise de Lindemann
2.0mm
Laser marking :
Depth : 10mm
Drill length : L
Reference mark
Depth : 10mm
REMOVE THE STOP AFTER USE, USING THE DEVICE INCLUDED IN THE KIT.
23
Identify the chin foramen and the inferior dental nerve to avoid accidental injury.
Using the drill guide, mark the position of the drill hole with the
round bur or the pointer drill.
The oblique lines on each end of the drill guide indicate a 30 orientation (Figure A).
Hold the drill parallel to the oblique line.
For an Axiom REG implant, refer to the drill sequence illustrated on
page 11, and for an Axiom PX implant, refer to the drill sequence
illustrated on page 14.
For placement of an Axiom REG in D1 bone type, prior tapping may
be necessary. The protocol is described on page 9.
Screw the implants into the prepared holes with the three-lobes
properly positioned relative to the prosthetic restoration
24
30
25
30
26
Tighten the MU Black Tite M1.6 screw using the long hexagonal
wrench.
Tighten to 25 N.cm: using the dynamometric ratchet wrench and
the hexagonal key, or the TORQ CONTROL hexagonal chuck.
27
28
3. Prosthetic protocols:
Axiom the new dimension
The Axiom prosthetic range is common to implants Axiom REG and Axiom PX.
The prosthetic range of the Axiom dental implant system is comprehensive. It allows the making of singleunit or multiple-unit, cemented or screw-retained prostheses, as well as the overdenture stabilisation.
With its unique prosthetic connection ( 2.7 mm), the Axiom prosthetic range is compatible with all Axiom REG and
Axiom PX implants.
In order to optimise aesthetics, the abutments are available in several emergence profile diameters, calibrated on the
diameters of the healing screws. The previous table selection of the healing screw (see p. 20), provides guidelines for
the selection of the appropriate diameter.
Some prosthetic components such as the standard titanium abutments (cemented prosthesis) and conical abutments
(screw-retained prosthesis) are supplied sterile for immediate, final placement in the mouth.
Reduced handlings helps not only to preserve peri-implant tissue but also to shorten the treatment time.
Ht. 1.5
Ht. 2.5
Ht. 3.5
Ht. 4.5
3.4
4.0
5.0
6.0
Constant emergence profile between the several prosthetic components, from the healing screw to the final abutment.
29
1. INDICATIONS
Delivered non sterile
Impression of the Axiom REG and Axiom PX implants on the healed site.
Recording of the precise healed gingival profile.
4.0
OPHS410
or
OPHSF410
OPHS420
or
OPHSF420
4.0
4.0
OPHS430
OPHS440*
or
or
OPHSF430 OPHSF440*
5.0
5.0
OPHS510
or
OPHSF510
OPHS520
or
OPHSF520
5.0
5.0
OPHS530
OPHS540*
or
or
OPHSF530 OPHSF540*
* It should be noted that H2.5 rings are compatible with emergence profiles H2.5 and H4.5.
3. EQUIPMENT REQUIRED
30
Hexagonal keys
Pick-up Transfer
Transfer screw
Pick-up Transfer L
Transfer screw
Impression rings
4.0 and 5.0
Remove the healing screw (or temporary abutment) using the hexagonal key.
Apply the impression ring corresponding to the emergence profile selected for a Pick-up New Design transfer Ref. OPPU100 or OPPU100L. The impression ring must be in contact with the first transfer fin (see diagram below with Pick-up Ref.
OPPU100). Place the Pick-up transfer in the implant and tighten the transfer screw (manual tightening). A reference marker should be used to check the correct position of the transfer in the implant.
OK
Landmark visible if
the transfer is set
up correctly.
NO
31
VISUAL
Single-unit Multiple-Unit
Fullarch
Sealed
Screwed
INDICATIONS
PAGE
Immediate
prosthetic
temporisation.
Removable.
33
Aesthetic
restoration.
Removable.
35
All-ceramic
restoration.
37
Immediate or
delayed placement .
Removable.
39
Reworkable abutment
4.0 mm
Temporary
abutments (sterile)
3.4, 4.0, 5.0, 6.0 mm
Aesthetic titanium
abutments
3.4, 4.0, 5.0, 6.0 mm
Aesthetic zirconia
abutments
5.0 mm
Standard titanium
abutments (sterile)
3.4, 4.0, 5.0, 6.0 mm
Gold-cast-on
abutment
41
43
Titanium base
Removable
45
Multi-Unit common
platform 4.8 mm
straight and angulated
46
Multi-Unit narrow
platform 4.0 mm
straight abutments
54
Pacific system on
Multi-Unit narrow
platform 4.0 mm
Conical abutments
Straigth 4.0 mm
Angulated 4.8 mm
Pacific system on
straight conical OPSC
abutment
LOCATOR abutments
4.0 mm
Screw-retained
restoration with
Multi-Unit narrow
abutments.
60
62
Screw-retained
restoration with
straight conical
abutments.
66
Overdenture
Stabilisation.
68
WARNING !
32
The emergence profile must not be altered in order to maintain the surface state of the gingiva. All final components
assembled on the implant are fixed by tightening to 25 N cm, except the healing screws and closure screw (manual tightening 5-10 N.cm). Altering the prosthetic components may compromise the mechanical resistance of the prosthetic reconstruction and thereby cause the implant to fail. This type of implant (type, diameter) must be selected according to
the type of restoration and the region.
4.0
5.0
6.0
EMERGENCE PROFILE
2. CHOICE OF ABUTMENT
Select the abutment from the 5 available gingival heights (0.75, 1.5, 2.5, 3.5 and 4.5 mm) and the 4 emergence profiles
(3.4 / 4.0 / 5.0 / 6.0 mm).
The abutment is ideally chosen depending on the emergence profile.
NOTE : try-in abutments are also available to help in the choice of gingival height.
3. EQUIPMENT REQUIRED
Hexagonal
mandrels
Hexagonal keys
M1.6 prosthetic
screw
Laboratory screw
4. USER PROTOCOL
hexagonal mandrels.
Close the access cavity(ies) with filling material after protecting the head of the screw.
WARNING !
34
When immediate loading procedure is not planned, it is essential to position the temporary prosthesis in sub-occlusion pending the final prosthesis, in order to ensure integrity of the
device.
3.4
4.0
5.0
6.0
EMERGENCE PROFILE
2. SELECTION OF ABUTMENT
Select the abutment from the 5 gingival heights (0.75, 1.5, 2.5, 3.5 and 4.5 mm), the 4 prosthesis emergence profiles
(3.4, 4.0, 5.0 and 6.0 mm) and 4 coronary angulation (0, 7, 15 and 23) available. Ideally, the abutment is chosen depending on the healing screw in situ, observing the concept of preserving the emergence profile.
NOTE : Try-in abutments are available to facilitate the choice of the abutment. Straight and angulated abutments follow
the same protocol of use. When using aesthetic abutments, take into consideration the implant orientation.
NOTE : AESTHETIC titanium abutments with Gh 4.5mm have a specific gingival profile to be used in the following situations :
- Gingival height of 4.5 mm and coronary height of 7 mm.
- Gingival height of 2.5 mm and coronary height of 9 mm.
In order to obtain this abutment with a coronary height of 9 mm the laboratory should rework the 2 mm cylindrical part.
Hexagonal
mandrels
Hexagonal keys
M1.6 prosthetic
screw
Pick-up
Transfer
Pop-in
Transfers
Implant
analog
3. EQUIPMENT REQUIRED
4. USER PROTOCOL
IMPRESSION-TAKING:
or
Take an impression using a closed impression tray (Pop-in technique) or open impression tray (Pick-up technique).
Re-insert the healing screw selected or make a temporary pros- PICK-UP
thesis using the temporary abutment (see p. 33)
POP-IN
35
PICK-UP
POP-IN
E TORQ CONTROL .
RESTORATION :
36
EMERGENCE PROFILE
2. SELECTION OF ABUTMENT
Select the abutment from the 2 gingival heights (1.5 and 3.5 mm) and 2 coronary angulations (0 and 15) available.
Ideally the abutment is chosen depending on the healing screw in situ, observing the concept of preserving the emergence
profile.
NOTE : try-in abutments are available to facilitate the choice of abutment.
3. EQUIPMENT REQUIRED
Hexagonal
mandrels
Hexagonal keys
M1.6 prosthetic
screw
Pick-up
Transfer
Pop-in
Transfers
Implant
analog
4. USER PROTOCOL
IMPRESSION-TAKING :
or
Re-insert the healing screw in situ or make a temporary prosthesis using the temporary abutment (see. p. 33).
PICK-UP
POP-IN
37
E TORQ CONTROL .
RESTORATION :
Close the access cavity(ies) with a filling material after protecting the screw head.
Seal the crown definitively onto the abutment in the mouth.
38
3.4
4.0
5.0
6.0
The standard titanium abutment is supplied decontaminated and sterilised with its fixation screw for direct placement in the mouth.
The impression is taken from the abutment in order to reduce the parodontal manipulations.
The recommended tightening torque for the standard titanium
abutment fixation screw is 25 N.cm.
Removable using the abutment extractor instrument
WARNING !
Do not re-work the abutment, in order not to compromise the impression
taking. If re-working is performed, take the conventional impression directly on the implant or take a conventional impression onto abutment.
EMERGENCE PROFILE
2. SELECTION OF ABUTMENT
Select the abutment from the 3 gingival heights (1.5, 2.5 and 3.5 mm), the 2 coronary heights (4.0 and 6.0 mm) and the 2
possible angles of angulated abutment non indexed (15and 23) available. The abutment is ideally chosen depending on
the healing screw in situ and observing the concept of emergence profile preservation. Select the abutment in order that no
re-working is required.
NOTE : try-in abutments are available to facilitate the choice of the abutment. Straight and angulated abutments follow the
same protocol of use. When using angulated abutments, take into consideration the implant orientation.
3. EQUIPMENT REQUIRED
Hexagonal
mandrels
Hexagonal keys
Impression
transfer
Protective cap
Rotational and
non-rotational
castable caps
Abutment
analog
4. USER PROTOCOL
nal mandrels.
39
Place the impression transfer on the top of the standard titanium abutment.
Maintain slight pressure, applying rotation to index the transfer
with the abutment.
Once the indexation is in place, press the transfer onto the nonre-worked abutment until it clicks.
Take a conventional impression using a standard impression
tray.
Once the impression has been taken, close the access cavity
with filling material after protecting the screw head.
Insert the abutment analog in the transfer into the impression intrados (until a click is heard) after visualising the
relative position of the analog in the impression.
Check that the analog is correctly fixed in the impression
(if necessary, repeat the procedure) and pour the master
model.
Fashion the metal frame using the castable coping. Cover
the analogs crown with spacer (necessary to stabilise the
castable coping).
Prepare the final prosthesis according to current restoration protocols.
Close the access cavity(ies) with a filling material after
protecting the screw head. Cement the crown with temporary cement onto the abutment in the mouth.
NOTE : rotational or anti-rotational castable copings are
available depending on the cement retained prosthesis (for
multiple or unit procedures respectively).
40
4.0 H1.5
EMERGENCE PROFILE
2. EQUIPMENT REQUIRED
Hexagonal
mandrels
Hexagonal keys
M1.6
prosthetic
screw
Laboratory screw
Pick-up
Transfer
Pop-in
Transfers
Implant
analog
3. USER PROTOCOL
IMPRESSION-TAKING :
Re-insert the healing screw in situ or make a temporary prosthesis using the temporary abutment (see. p. 33).
WARNING !
The single size of the gold cast-on abutment has a single dimension of healing screw. Observe the concept of preservation of the
emergence profile.
PICK-UP
POP-IN
41
Insert, indexing the gold cast-on abutment into the implant in the
correct orientation and screw the Black Tite M1.6 fixation screw
supplied.
A retro-alveolar x-ray may be performed to confirm that the
abutment is completely connected to the implant.
Tighten at 25 N.cm using the dynamometric ratchet wrench or
E TORQ CONTROL .
RESTORATION :
POP-IN
4.0 H1.5
EMERGENCE PROFILE
2. EQUIPMENT REQUIRED
Hexagonal
mandrels
Hexagonal keys
M1.6 prosthetic
screw
Pick-up
Transfer
Pop-in
Transfers
Implant
analog
3. USER PROTOCOL
IMPRESSION-TAKING :
WARNING !
The single size of the reworkable abutment has a single dimension of healing screw.
or
PICK-UP
POP-IN
43
E TORQ CONTROL .
RESTORATION :
44
POP-IN
4.5
4.0
5.0
The titanium base is delivered decontaminated and non sterile with its
fixing screw.
The titanium base must not be altered (either on the gingival part or
the coronary part). Any alteration risks weakening the mechanical
structure of the part. The coronary part will only tolerate corundum
blasting (Al203) with a granulometry between 50m and 125m and with
pressure of 2 to 4 bars where blasting is required by the manufacturer
of the adhesive materials.
Recommended tightening for the titanium base screw is 25 N.cm.
The Axiom S Tibase L titanium base is compatible only with size L
machining blocks marketed by Sirona.
Axiom - S Tibase L
Flexibase Axiom
EMERGENCE PROFILE
2. CHOICE OF TIBASE
Flexibase Axiom titanium bases are used in the laboratory to create single-tooth abutments and screw-retained dentures.
They can be selected from two possible diameters (4.0 / 5.0 mm).
The Axiom S Tibase L titanium base is made of a coronary part that is compatible with the CEREC digitised caps and
machine attachments marketed by Sirona.
4.8
4.0
The recommended torque for 4.8 mm and 4.0 mm Multi-Unit abutments is 25 N.cm.
Connection of angled Multi-Unit abutments to Axiom REG/PX implants is performed using a dedicated Multi-Unit M1.6
fixation screw.
= 4.8 mm
CH = 2.5 mm
= 4.8 mm
GH
20
= 4.0 mm
CH = 2.5 mm
GH
CH = 1.5 mm
GH
46
4.8 mm and 4.0 mm straight Multi-Unit abutments should be tightened at 25 N.cm either with
the Multi-Unit mandrel MUM100 or the Multi-Unit wrench MUW100.
Connection of temporary or permanent auxiliary components to Multi-Unit abutments requires the use of the dedicated
Multi-Unit M1.4 fixation screws using a torque of 15 N.cm. Protective caps must be hand tightened. Multi-Unit M1.4 fixation screws are compatible with both 4.8 mm and 4.0 mm platforms. A color coding system is used for all auxiliary components for 4.8 mm and 4.0 mm Multi-Unit abutments:
Laboratory screws (Multi-Unit titanium M1.4 screws and Multi-Unit laboratory screws)
for use with 4.8 mm and 4.0 mm Multi-Unit abutments: Blue color code.
Components for use with 4.8 mm Multi-Unit abutments: Yellow color code on whole or part of the component.
Components for use with 4.0 mm Multi-Unit abutments: Green color code on whole or part of the component.
Components for 4.0 mm Multi-Unit abutments are lasermarked N for Narrow .
AUXILIARY COMPONENTS INTENDED FOR USE WITH MULTI-UNIT COMMON PLATFORM 4.8 MM
Multi-Unit
Pick-up
Transfer
4.8mm
Multi-Unit
Pop-in
Transfer
4.8mm
Multi-Unit
implant
analog
4.8mm
Multi-Unit
protective
analog
4.8mm
Temporary
Multi-Unit
titanium
protective cap Multi-Unit
4.8mm
cap 4.8mm
Temporary
Multi-Unit
PEEK cap
4.8mm
Castable
PMMA
Multi-Unit
cap 4.8mm
CoCr
Multi-Unit
cap 4.8mm
AUXILIARY COMPONENTS INTENDED FOR USE WITH MULTI-UNIT NARROW PLATFORM 4.0 MM
Multi-Unit
Pick-up
Transfer
4.0mm
Multi-Unit
Pop-in
Transfer
4.0mm
Multi-Unit
implant
analog
4.0mm
Multi-Unit
protective
analog
4.0mm
Temporary
Multi-Unit
titanium
protective Multi-Unit cap
cap 4.0mm
4.0mm
Temporary
Multi-Unit
PEEK cap
4.0mm
Castable
CoCr
PMMA
Multi-Unit cap Multi-Unit cap
4.0mm
4.0mm
47
4.8
EMERGENCE PROFILE
In case of Axiom REG/PX healing screw placement before Multi-Unit common platform 4.8 abutment placement, it is
recommended to use a 5.0 mm healing screw in order not to compress the gum during the conical abutments placement.
When using OPMU0-4 abutments, a healing screw (Ref.OPHS530) may be used during the healing phase.
When the laboratory realises a multiple-unit prosthesis from a master-model with implant analogs, he must use MultiUnit Blue M1.6 screws (Art. Nb. OPMU161) supplied unitary.
WARNING !
Multi-Unit screws and auxiliary components should be used with Multi-Unit abutments only, and must not be used with
OPSC/OPAC conical abutments. Mixing Multi-Unit and OPSC/OPAC components or screws may result in improper fit of
the restoration.
The handpiece provided with Multi-Unit abutments can be used to facilitate placing of the abutment. This handling tool
must absolutely not be used to tighten the straight Multi-Unit abutment into the implant with a torque of 25 N.cm. Do not
apply a torque greater than 5 N.cm to this handling tool.
48
4. EPUIPMENT REQUIRED
Handling tool
Hexagonal
mandrels
Hexagonal
keys
Multi-Unit
protective
analog
4.8mm
Temporary
Castable
Temporary
CoCr
titanium
PMMA
Multi-Unit
Multi-Unit
Multi-Unit
protective cap Multi-Unit PEEK cap Multi-Unit
cap
cap
cap
4.8mm
4.8mm
4.8mm
4.8mm 4.8mm
5. USER PROTOCOL
WARNING !
Before placing the MULTI-UNIT ABUTMENT in the patients mouth, make sure that the MULTI-UNIT HOLDER is securely
fixed.
For reduced mouth openings, unscrew the handpiece provided with the Multi-Unit abutment and screw on the short handle (Ref. MUWS)
49
Place a Multi-Unit Pick-up (MUT100) or Pop-in transfer (MUT200) on each conical abutment, and secure it by
inserting and hand tightening (using moderate force) a
short or long transfer screw.
PICK-UP
POP-IN
PICK-UP
LABORATORY :
TEMPORARY PROSTHESIS
50
POP-IN
WARNING !
Unless immediate loading is performed, the provisional
should be placed out of occlusion so as not to compromise
device integrity.
51
Try-in
Remove the protective caps or the provisional to try in
the poured component. In particular, check for good fit
and secure fixation of the component (hand tighten the
Multi-Unit titanium M1.4 fixation screws to 5-10 N.cm).
Multi-Unit protection analogs (MUA200) are available
to protect the Multi-Unit connection system during fabrication of the final restoration.
In the mouth
52
Tighten to 15 N.cm using the dynamometric prosthesis key Ref. INCCD or using TORQ CONTROL.
53
4.0
WARNING !
Multi-Unit screws and auxiliary components should be used with Multi-Unit abutments only, and must not be used with
OPSC/OPAC conical abutments. Mixing Multi-Unit and OPSC/OPAC components or screws may result in improper fit of
the restoration.
The handling tool provided with Multi-Unit abutments can be used to facilitate placing of the abutment. This handle must
absolutely not be used to tighten the straight Multi-Unit abutment into the implant with a torque of 25 N.cm. Do not apply
a torque greater than 5 N.cm to this handle.
4. EQUIPMENT REQUIRED
Handling tool
54
Hexagonal
mandrels
Hexagonal
keys
Multi-Unit
Pick-up
Multi-Unit
mandrel and Transfer
abutment key 4.0mm
Multi-Unit
Pop-in
Transfer
4.0mm
Multi-Unit
abutment
analog
4.0mm
Multi-Unit
protective
analog
4.0mm
Temporary
Castable
Temporary
CoCr
titanium
PMMA
Multi-Unit
Multi-Unit
Multi-Unit
protective cap Multi-Unit PEEK cap Multi-Unit
cap
cap
cap
4.0mm
4.0mm
4.0mm
4.0mm 4.0mm
5. USER PROTOCOL
WARNING !
Before placing the MULTI-UNIT ABUTMENT in the patients mouth, make sure that the MULTI-UNIT HANDLING
TOOL is securely fixed.
For reduced mouth openings, unscrew the handling tool
provided with the Multi-Unit abutment and screw on the
short handle (Ref. MUWS)
PICK-UP
POP-IN
PICK-UP
POP-IN
LABORATORY :
55
TEMPORARY PROSTHESIS :
WARNING !
Unless immediate loading is performed, the provisional
should be placed out of occlusion so as not to compromise device integrity.
56
Try-in
Remove the protective caps or the temporary prosthesis to try in the casted component. In particular,
check for good fit and secure fixation of the component
(hand tighten the Multi-Unit dedicated titanium M1.4
fixation screws to 5-10 N.cm).
Multi-Unit narrow 4.0 protection analogs (MUNA200)
are available to protect the Multi-Unit connection system during fabrication of the final restoration.
In the mouth
57
In the laboratory
In the mouth
59
4.0
EMERGENCE PROFILE
WARNING !
Multi-Unit screws and auxiliary components should be used with Multi-Unit abutments only, and must not be used with
OPSC/OPAC conical abutments. Mixing Multi-Unit and OPSC/OPAC components or screws may result in improper fit of
the restoration.
2. EQUIPMENT REQUIRED
M1.4 laboratory
screw
Hexagonal
mandrels
Hexagonal keys
M1.4 Multi-Unit
Narrow Pacific Narrow Multi-Unit Narrow Multi-Unit Long Multi-Unit
Black Tite fixing
Multi-Unit Analog
laboratory screw
bonding ring
castable cap
screw
3. USER PROTOCOL
Connect the Pacific Multi-Unit narrow analogs (Ref. MUNPAC110) onto the conical abutments analogs using the MultiUnit laboratory screw M1.4 (Ref. MU141, moderate manual
tightening).
Use a hexagonal wrench.
60
Place the Multi-Unit narrow castable copings (Ref. MUNPAC120) onto the narrow Multi-Unit Pacific analogs, adjust
them so as to recreate a madeto-measure homothetic framework (or castable bar) by drilling and/or addition of castable
resin by connecting each coping.
Perform casting in compliance with the material manufacturers recommendations. Proceed with the assembly and firing
of the ceramic on the framework. Carry out finishing work.
Sand and clean the basal surface of the prosthesis.
CHECKING PASSIVITY:
nal mandrel.
61
The recommended tightening torque for the fixation screws for the
angulated and straight conical abutments is 25 N.cm, the recommended
torque for the secondary components is 15 N.cm.
EMERGENCE PROFILE
WARNING !
Multi-Unit screws and auxiliary components should be used with Multi-Unit abutments only, and must not be used with
OPSC/OPAC conical abutments. Mixing Multi-Unit and OPSC/OPAC components or screws may result in improper fit of
the restoration.
4. EQUIPMENT REQUIRED
STRAIGHT CONICAL ABUTMENT :
M1.4
laboratory
screw
(1)
Hexagonal
mandrels
62
Hexagonal
keys
Straigh
conical
abutment
mandrel
Straight
conical
abutment
wrench
Pick-up
Transfer
Pop-in
Transfer
Abutment
analog
Protective
cover
Black Tite
M1.4 fixation Temporary
cap
screw
Ceramicor
Castable
gold overcascap
table cap
Hexagonal
mandrels
Hexagonal
keys
M1.6 Black
Tite prosthetic
screw
Pick-up
Transfer
Pop-in
Transfer
Protective
cover
Black Tite
Ceramicor
M1.4 fixation Temporary Castable cap gold overcascap
screw
table cap
5. USER PROTOCOL
Abutment
analog
(2)
PICK-UP
POP-IN
Assemble each Pick-up or Pop-in transfer respectively onto each conical abutment and screw the
transfer screw (moderate manual tightening).
Take an impression using a closed impression
tray (Pop-in technique) or open impression tray
(Pick-up technique).
Replace the protective covers with moderate
manual tightening or make a temporary prosthesis
with the appropriate copings (Cf.Temporary prosthesis).
PICK-UP
POP-IN
LABORATORY :
63
TEMPORARY PROSTHESIS
(AFTER IMPRESSION TAKING) :
WARNING !
If immediate loading is not planned, it is recommended
that the temporary prosthesis be positioned in subocclusion pending the definitive prosthesis in order to
guarantee integrity of the device.
64
65
4.0
The bonding ring can only be used with straight conical abutments.
WARNING !
Multi-Unit screws and auxiliary components should be used with Multi-Unit abutments only, and must not be used with
OPSC/OPAC conical abutments. Mixing Multi-Unit and OPSC/OPAC components or screws may result in improper fit of
the restoration.
2. EQUIPMENT REQUIRED
M1.4 laboratory
screw
Hexagonal
mandrels
Hexagonal keys
Pacific
Analog
Castable
cap
Bonding
unit
3. USER PROTOCOL
66
Short conical
abutment
pick-up screw
Long conical
abutment
pick-up screw
CHECKING PASSIVITY :
nal mandrel.
67
1. INDICATIONS
Supplied non sterile
Stabilisation of a partial implant-supported restoration,
overdenture stabilisation.
LOCATOR attachments (Clear, Pink, Blue) can correct divergence
up to 20between two implants.
Extended range attachments (Red, Green, Orange, Grey)
can correct divergence up to 40 between 2 implants.
4.0
4.0
4.0
OPHS410
OPHS420
OPHS430
OPHS440
or
or
or
or
OPHSF410 OPHSF420 OPHSF430 OPHSF440
4.0
OPHS440
OPLA010
GH : 1.5
OPLA020
GH : 2.5
OPLA030
GH : 3.5
OPLA040
GH : 4.5
OPLA050
GH : 5.5
EMERGENCE PROFILE
Choose the abutment from the 5 gingival heights (1.5, 2.5, 3.5, 4.5 and 5.5 mm) for 1 single emergence
diameter ( 4.0mm) available. The selection of the LOCATOR abutment will depend on the healing screw in
place, and the emergence profile will have to be preserved. The LOCATOR abutment can also be used during
the healing stage.
A 5.5 mm high LOCATOR abutment requires the use of a healing screw OPHS440.
3. EQUIPMENT REQUIRED
LOCATOR
mandrel
LOCATOR
wrench
LOCATOR transfer +
nylon (black)
LOCATOR
analog
3 in 1 tool
4. USER PROTOCOL
Direct or indirect technique can be used with the LOCATOR abutment.
INDIRECT TECHNIQUE
Placement of LOCATOR abutment
Screw the LOCATOR abutment into the implant using the LOCATOR wrench, the ratchet wrench or TORQ CONTROL.
68
Restoration procedure
For less than 20 degrees of divergence between 2 implants (up to 10 per implant)
STANDARD
RETENTION
MEDIUM
RETENTION
LOW
RETENTION
Clear attachment
(2268g - 5Lbs)
Pink attachment
(1361g - 3.0Lbs)
Blue attachment
(680g - 1.5Lbs)
LIGHT
RETENTION
EXTRA-LIGHT
RETENTION
RTENTION
ZRO
Green attachment
(1361-1814g - 3.0-4.0Lbs)
Orange attachment
(907g - 2.0-0Lbs)
Red attachment
(226-680g - 0.5-1.5Lbs)
Grey attachment
(0Lbs)
Spacer ring
Black housing
3 in 1 tools
Abutment driver
69
70
Hexagonal wrenches
short and long
Dynamometric ratchet
wrench INCCD
Hexagonal mandrels
short and long
*
Multi-Unit mandrel
Multi-Unit wrench
The XL hexagonal key and the INEXPL abutment extractor must be positioned in the
centre of the set. (locations* shown in photo)
Dynamometric ratchet wrench: torque values (N.cm) 15/25/35. Precision (N.cm) +/- 2.
Instructions for use available on request.
TECHNICAL SPECIFICATIONS
The kit is designed using medical grade materials enabling it to tolerate heat disinfection
and autoclave sterilisation.
The protective covers provide flexibility when positioning the kit in order to optimise
instrument accessibility .
71
INEXPS
Abutment
extractor
INEXPL
Abutment
gripper
1. EXTRACTOR FUNCTION
The abutment extractor is available in two lengths: short and long. It allows
the removal of AXIOM REG/PX abutments that include the statement
Extractible/Removable on the traceability label provided on the blister
packaging of the abutment:
These abutments feature a specific internal screw thread that is compatible with the abutment extractor instrument. It can be used in the dental
surgery or laboratory whenever an abutment is to be replaced or modified.
This instrument allows very simple removal of abutments featuring an internal screw thread, without damaging the implant-prosthesis connection
and without subjecting the assembly to force or stress.
Wheel
Abutment extractor body
Fit the rod inside the body of the extractor and screw
in the wheel, leaving a gap of 2mm (approx.) between the
head of the extractor and the wheel
72
2mm
To clean the instrument, disassemble by unscrewing the body of the extractor and the rod.
Information on the cleaning protocol is provided in section4 Cleaning and sterilization (see p.70)
2. GRIPPING FUNCTION
The instrument can also be used to enable abutment placement in the mouth, including areas that are difficult to access.
Only the body of the extractor is used to apply this gripping function.
Screw the body of the extractor into the abutment
73
A. GENERAL INFORMATION
All cleaning-disinfection and sterilisation protocols must be followed by correctly trained protected staff in accordance
with current regulations. In order to avoid any risk of infection or injury, it is essential that appropriate clothing be worn
(protective mask, gloves and glasses).
following the protocol, it is mandatory to follow current regulations, referring to the Good Hospital Pharmacy
D When
Practice recommendations, the Good Disinfection Practice guide, the Good Sterilisation Practice Guide and the
guide for correct execution of treatments applying to reusable medical devices in reference FD S98-135 of April 2005.
All cleaning-disinfection and sterilisation protocols must be appropriate for the risks of infection. The user or medical
staff must ensure that the protocol used achieves the sterility objective. The protocol must enable all chemical and organic residues on the treated device to be removed (in particular ensure that used products are correctly rinsed).
WARNING !
For aluminium alloys, the use of sodium hydroxide solution is strictly prohibited.
For the stainless steels, the use of sodium hypochlorite (bleach) is strictly prohibited : high risk of corrosion.
Drills and taps should never be cleaned with hydrogen peroxide [H 202] as there is a risk of chemical stripping.
The material composition of each component and full list of the part numbers can be found at the end of this
D document.
74
B. PRODUCTS
1. DETERGENT-DISINFECTANT PRODUCTS
In order to guarantee sufficient decontamination before sterilisation, the detergents and disinfectants must be chosen
according to the risks of infection depending on their field of activity : standard microbial activity (bacteria, fungicide,
virucide) and their cleaning capacity.
The detergents and disinfectants used must be consistent with the cleaning method used.
The user must refer to the manufacturers instructions for each cleaning and disinfecting product :
Observe the concentrations, temperatures and exposure times.
Observe solution replacement and lifespan of the products.
Observe instructions for disposal of used products.
Never mix products.
WARNING !
Do not use substances liable to bind proteins (alcohol, aldehydes, etc.).
more information, the user may refer to guide FD S98-135, the Guide for prevention of healthcare related
D For
infections in dental surgery and stomatology July 2006 and the positive list of dental disinfectants 2009 published
by SFHH and ADF
2. WATER QUALITY
The water used for pre-disinfection, cleaning, decontamination, rinsing and sterilisation must meet current regulations.
The user may refer to document FD S 98-135 9-4.
The water quality must be compatible with the sterility objective and equipment used.
It is important that conductivity, pH, water hardness, ion and impurity concentration and microbiological pollution be monitored.
WARNING !
Any used component intended to be returned to the after sales service must be sent sterile after pre-disinfection, cleaning and decontamination in accordance with current legislation, with proof of sterility.
75
C. PROTOCOLS
1. PRE-DISINFECTION
Pre-disinfection must be performed immediately after each surgery on all dismantled re-usable components (See Instructions for dismantling and assembly p.78) :
Pre-disinfect separately, detaching systematically whenever possible all assembled devices.
Completely immerse in the pre-disinfection solution.
Rinse with osmosed, demineralized water to avoid any deposits.
Carefully dry immediately with soft, sterile wipes (combined with medical grade compressed air).
2. CLEANING DISINFECTION
Dismantled components must be cleaned separately (kits and dismantlable ratchet keys, (See Dismantling and Assembly
Instructions , p.78).
Cleaning by brushing
Brush meticulously with a soft brush (for example nylon).
Completely immerse in a detergent disinfectant solution following the manufacturers recommendations.
Rinse with osmosed, demineralized water to avoid any deposits.
Carefully dry immediately with soft, sterile, fluffless wipes (combined with medical grade compressed air).
Check the result and repeat the cleaning procedure if necessary.
WARNING !
Do not place cutting instruments in contact during ultrasound cleaning.
Rubbing of the parts against each other or against the tank may cause defects in appearance.
76
4. STERILISATION
A prior cleaning-disinfection and drying are required before sterilisation of components (+pre-disinfection for reusable
components).
Place each component in an individual sealed pouch (NF EN ISO 11607) suitable for steam sterilisation.
Complete surgical kits should be packed in flat sterilisation packaging pouches (with covers closed).
Use the following parameters for a steam autoclave: 135C (275F), 2.13 bars (30,88 psi), 20-minute minimum exposure
time.
Both sterilisation date and expiry date should be mentioned on the pouches. The expiration date should be in accordance
with the target shelf life established for each type of packaging under specific storage conditions (one month maximum).
WARNING !
Only use the above sterilisation methods for sterilisation of instruments, components, and accessories.
Anthogyr recommends using class B autoclaves.
Manufacturers recommendations for use and maintenance of the autoclave should always be followed.
Place the pouches so that they do not collide during the sterilisation procedure.
Strictly follow the recommendations of the pouch manufacturer regarding storage conditions of sterile components.
77
B. INSTRUMENT KIT
Insert 3/4
Insert 1/4
Remove the side cover ends around the stainless steel plates.
Detach the silicone cover plates.
78
REFERENCES
Axiom REG
Implant 3.4 mm
Prosthetic interface 2.7 mm
STERILE
3.4 x 8 mm
3.4 x 10 mm
3.4 x 12 mm
3.4 x 14 mm
3.4 x 16 mm
3.4 x 18 mm
OP34080
OP34100
OP34120
OP34140
OP34160
OP34180
Axiom REG
Implant 4.0 mm
Prosthetic interface 2.7 mm
STERILE
4.0 x 6.5 mm
4.0 x 8 mm
4.0 x 10 mm
4.0 x 12 mm
4.0 x 14 mm
4.0 x 16 mm
4.0 x 18 mm
OP40060
OP40080
OP40100
OP40120
OP40140
OP40160
OP40180
Axiom REG
Implant 4.6 mm
Prosthetic interface 2.7 mm
STERILE
4.6 x 6.5 mm
4.6 x 8 mm
4.6 x 10 mm
4.6 x 12 mm
4.6 x 14 mm
OP46060
OP46080
OP46100
OP46120
OP46140
Axiom REG
Implant 5.2 mm
Prosthetic interface 2.7 mm
STERILE
80
5.2 x 6.5 mm
5.2 x 8 mm
5.2 x 10 mm
5.2 x 12 mm
5.2 x 14 mm
OP52060
OP52080
OP52100
OP52120
OP52140
IMPLANTS
REFERENCES
Axiom PX
Implant 3.4 mm
Prosthetic interface 2.7 mm
STERILE
3.4 x 8 mm
3.4 x 10 mm
3.4 x 12 mm
3.4 x 14 mm
3.4 x 16 mm
3.4 x 18 mm
PX34080
PX34100
PX34120
PX34140
PX34160
PX34180
Axiom PX
Implant 4.0 mm
Prosthetic interface 2.7 mm
STERILE
4.0 x 8 mm
4.0 x 10 mm
4.0 x 12 mm
4.0 x 14 mm
4.0 x 16 mm
4.0 x 18 mm
PX40080
PX40100
PX40120
PX40140
PX40160
PX40180
Axiom PX
Implant 4.6 mm
Prosthetic interface 2.7 mm
STERILE
4.6 x 6.5 mm
4.6 x 8 mm
4.6 x 10 mm
4.6 x 12 mm
4.6 x 14 mm
PX46060
PX46080
PX46100
PX46120
PX46140
Axiom PX
Implant 5.2 mm
Prosthetic interface 2.7 mm
STERILE
5.2 x 6.5 mm
5.2 x 8 mm
5.2 x 10 mm
5.2 x 12 mm
PX52060
PX52080
PX52100
PX52120
81
B. SURGICAL INSTRUMENTS
DRILLS AND TAPS
REFERENCES
Round bur
Medical grade stainless steel
Round bur
INFB20
Pointer drill
Medical grade stainless steel
Pointer drill
OPPO15150
Lindemann bur
Medical grade stainless steel
Lindemann bur 2.0
OPR20
Initial drills
Medical grade stainless steel
Initial drills 2.0 S
Initial drills 2.0 L
OPFI20S
OPFI20L
Step drills
Medical grade stainless steel
S Drills
Step drills 2.0 /2.4 S
Step drills 2.4 /3.0 S
Step drills 3.0 /3.6 S
Step drills 3.6 /4.2 S
Step drills 4.2 /4.8 S
Pack of 6 S drills (initial drill 2.0 S + 5 S drills)
OPFE24S
OPFE30S
OPFE36S
OPFE42S
OPFE48S
OPFES-6
L Drills
Step drills 2.0 /2.4 L
Step drills 2.4 /3.0 L
Step drills 3.0 /3.6 L
Step drills 3.6 /4.2 L
Step drills 4.2 /4.8 L
Pack of 6 L drills (initial drill 2.0 L + 5 S drills)
OPFE24L
OPFE30L
OPFE36L
OPFE42L
OPFE48L
OPFEL-6
OPFESL-12
82
OPTA34L
Tap 4.0 mm
Axiom REG Tap
OPTA40L
Tap 4.6 mm
Axiom REG Tap
OPTA46L
Tap 5.2 mm
Axiom REG Tap
OPTA52L
Pack of 4 L taps
OPTA-4
REFERENCES
17 mm
21 mm
26 mm
OPMV180
OPMV215
OPMV250
19 mm
25 mm
31 mm
OPCV060
OPCV110
OPCV160
INPIM
INPIL
INMHELV
OPCS100
Mandrel extension
Medical grade stainless steel
Mandrel extension
INEXM
INCPM
INCC
INCCDC
OPJC001
83
ACCESSORIES OF SURGERY
REFERENCES
Gauges
Medical grade V titanium
Gauge 2.0 mm
Gauge 2.4 mm
Gauge 3.0 mm
Gauge 3.6 mm
Gauge 4.2 mm
Gauge 4.8 mm
OPJD020
OPJD024
OPJD030
OPJD036
OPJD042
OPJD048
Drill guide
Medical grade stainless steel
Parallelising drill guide
INGPPA
SURGICAL KITS
INGFA
REFERENCES
INMODOPS2
84
KTDRILLOPS2
INMODOPS2V
OPFC_NOT
PXFC_NOT
REFERENCES
INKITOSTEOFULL
INKITOSTEOCC
INKITOSTEOCX
INMODOSTV
Straight osteotomes
Medical grade stainless steel
Straight concave osteotome 2.0 / 2.8
Straight concave osteotome 2.5 / 3.3
Straight concave osteotome 3.0 / 3.9
Straight concave osteotome 3.5 / 4.5
Straight convex osteotome 2.0 / 2.8
Straight convex osteotome 2.5 / 3.3
Straight convex osteotome 3.0 / 3.9
Straight convex osteotome 3.5 / 4.5
OSTSCC34
OSTSCC40
OSTSCC46
OSTSCC52
OSTSCX34
OSTSCX40
OSTSCX46
OSTSCX52
Bayonet osteotomes
Medical grade stainless steel
Concave bayonet osteotome 2.0 / 2.8
Concave bayonet osteotome 2.5 / 3.3
Concave bayonet osteotome 3.0 / 3.9
Concave bayonet osteotome 3.5 / 4.5
Convex bayonet osteotome 2.0 / 2.8
Convex bayonet osteotome 2.5 / 3.3
Convex bayonet osteotome 3.0 / 3.9
Convex bayonet osteotome 3.5 / 4.5
OSTECC34
OSTECC40
OSTECC46
OSTECC52
OSTECX34
OSTECX40
OSTECX46
OSTECX52
Osteotome set
OSTECX_SET
OSTECC_SET
OSTSCX_SET
OSTSCC_SET
INUSI
INEXMOST
OPMVTOST
85
DRILL STOPS
REFERENCES
OPB3006C
OPB3008C
OPB3010C
OPB3006L
OPB3008L
OPB3010L
OPB3012L
OPB3014L
OPB3016L
OPB3018L
OPB3606C
OPB3608C
OPB3610C
OPB3606L
OPB3608L
OPB3610L
OPB3612L
OPB3614L
OPB3616L
OPB3618L
OPB4206C
OPB4208C
OPB4210C
OPB4206L
OPB4208L
OPB4210L
OPB4212L
OPB4214L
OPB4806C
OPB4808C
OPB4810C
OPB4806L
OPB4808L
OPB4810L
OPB4812L
OPB4814L
REFERENCES
INKITOPDS
86
INKITOPDSV
C. PROSTHETIC COMPONENTS
Prosthetic components are delivered non-sterile, unless otherwise stated.
PROSTHETIC SCREWS
REFERENCES
Closure screw
STERILE
OPIM100
Healing screws
STERILE
3.4
3.4
3.4
3.4
H 1.5
H 2.5
H 3.5
H 4.5
OPHS310
OPHS320
OPHS330
OPHS340
4.0
4.0
4.0
4.0
4.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
OPHS400
OPHS410
OPHS420
OPHS430
OPHS440
5.0
5.0
5.0
5.0
5.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
OPHS500
OPHS510
OPHS520
OPHS530
OPHS540
6.0
6.0
6.0
6.0
H 1.5
H 2.5
H 3.5
H 4.5
OPHS610
OPHS620
OPHS630
OPHS640
3.4
3.4
3.4
3.4
H 1.5
H 2.5
H 3.5
H 4.5
OPHSF310
OPHSF320
OPHSF330
OPHSF340
4.0
4.0
4.0
4.0
4.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
OPHSF400
OPHSF410
OPHSF420
OPHSF430
OPHSF440
5.0
5.0
5.0
5.0
5.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
OPHSF500
OPHSF510
OPHSF520
OPHSF530
OPHSF540
6.0
6.0
6.0
6.0
H 1.5
H 2.5
H 3.5
H 4.5
OPHSF610
OPHSF620
OPHSF630
OPHSF640
87
REFERENCES
OPTS160
OPTS161
OPTS162
OPPU101
OPPU102
OPAC140
OPAC141
OPAC501
OPMU160
OPMU161
OPMU161-4
MU140
MU141
MUT101
MUT102
REFERENCES
4.0
4.0
4.0
5.0
5.0
5.0
GH 1.5
GH 2.5
GH 3.5
GH 1.5
GH 2.5
GH 3.5
OPROFIL410
OPROFIL420
OPROFIL430
OPROFIL510
OPROFIL520
OPROFIL530
Pick-up Transfer
Impression taken directly on the implant
OPPU100
OPPU100-4
88
OPPU100L
OPPU100L-4
REFERENCES
Pop-in transfer
Taking direct impression from implant
OPPI100S
OPPI100S-4
Implant analog
OPIA100
OPIA100-4
REFERENCES
STERILE
3.4
3.4
3.4
3.4
H 1.5
H 2.5
H 3.5
H 4.5
OPTP310
OPTP320
OPTP330
OPTP340
4.0
4.0
4.0
4.0
4.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
OPTP400
OPTP410
OPTP420
OPTP430
OPTP440
5.0
5.0
5.0
5.0
5.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
OPTP500
OPTP510
OPTP520
OPTP530
OPTP540
6.0
6.0
6.0
6.0
H 1.5
H 2.5
H 3.5
H 4.5
OPTP610
OPTP620
OPTP630
The temporary, standard, aesthetic and Flexibase abutments are Removable using the INEXPS or INEXPL gripper
89
PERSONALISABLE ABUTMENTS
REFERENCES
OPOG110
Reworkable abutment
OPFS100
Flexibase
Medical Grade V Titanium
Titanium base 4
Titanium base 5
OPFLEX403
OPFLEX503
PMMA
Castable coping 4
Castable coping 5
OPFLEXC403
OPFLEXC503
Axiom S Tibase L
Medical Grade V Titanium
Titanium base
OPBASE-S45
REFERENCES
90
3.4
3.4
3.4
3.4
H 1.5
H 2.5
H 3.5
H 4.5
7
7
7
7
OPAT31-7
OPAT32-7
OPAT33-7
OPAT34-7
3.4
3.4
3.4
3.4
H 1.5
H 2.5
H 3.5
H 4.5
15
15
15
15
OPAT311
OPAT321
OPAT331
OPAT341
REFERENCES
4.0
4.0
4.0
4.0
4.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
0
0
0
0
0
OPAT400
OPAT410
OPAT420
OPAT430
OPAT440
4.0
4.0
4.0
4.0
4.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
7
7
7
7
7
OPAT40-7
OPAT41-7
OPAT42-7
OPAT43-7
OPAT44-7
4.0
4.0
4.0
4.0
4.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
15
15
15
15
15
OPAT401
OPAT411
OPAT421
OPAT431
OPAT441
4.0
4.0
4.0
4.0
4.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
23
23
23
23
23
OPAT402
OPAT412
OPAT422
OPAT432
OPAT442
5.0
5.0
5.0
5.0
5.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
0
0
0
0
0
OPAT500
OPAT510
OPAT520
OPAT530
OPAT540
5.0
5.0
5.0
5.0
5.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
7
7
7
7
7
OPAT50-7
OPAT51-7
OPAT52-7
OPAT53-7
OPAT54-7
5.0
5.0
5.0
5.0
5.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
15
15
15
15
15
OPAT501
OPAT511
OPAT521
OPAT531
OPAT541
5.0
5.0
5.0
5.0
5.0
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
23
23
23
23
23
OPAT502
OPAT512
OPAT522
OPAT532
OPAT542
6.0
6.0
6.0
6.0
H 1.5
H 2.5
H 3.5
H 4.5
0
0
0
0
OPAT610
OPAT620
OPAT630
OPAT640
6.0
6.0
6.0
6.0
H 1.5
H 2.5
H 3.5
H 4.5
15
15
15
15
OPAT611
OPAT621
OPAT631
OPAT641
91
REFERENCES
5.0
5.0
H 1.5
H 1.5
0
15
5.0
5.0
H 3.5
H 3.5
0
15
STERILE
3.4
3.4
3.4
3.4
3.4
3.4
H 1.5/H 4
H 2.5/H 4
H 3.5/H 4
H 1.5/H 6
H 2.5/H 6
H 3.5/H 6
0
0
0
0
0
0
OPST314
OPST324
OPST334
OPST316
OPST326
OPST336
STD abutment
STD abutment
STD abutment
STD abutment
STD abutment
STD abutment
4.0
4.0
4.0
4.0
4.0
4.0
H 1.5/H 4
H 2.5/H 4
H 3.5/H 4
H 1.5/H 6
H 2.5/H 6
H 3.5/H 6
0
0
0
0
0
0
OPST414
OPST424
OPST434
OPST416
OPST426
OPST436
STD abutment
STD abutment
STD abutment
STD abutment
STD abutment
STD abutment
5.0
5.0
5.0
5.0
5.0
5.0
H 1.5/H 4
H 2.5/H 4
H 3.5/H 4
H 1.5/H 6
H 2.5/H 6
H 3.5/H 6
0
0
0
0
0
0
OPST514
OPST524
OPST534
OPST516
OPST526
OPST536
STD abutment
STD abutment
STD abutment
STD abutment
STD abutment
STD abutment
6.0
6.0
6.0
6.0
6.0
6.0
H 1.5/H 4
H 2.5/H 4
H 3.5/H 4
H 1.5/H 6
H 2.5/H 6
H 3.5/H 6
0
0
0
0
0
0
OPST614
OPST624
OPST634
OPST616
OPST626
OPST636
15
15
15
OPST416_15
OPST426_15
OPST436_15
H 1.5/H 6
H 2.5/H 6
H 3.5/H 6
15
15
15
OPST516_15
OPST526_15
OPST536_15
23
23
23
OPST416_23
OPST426_23
OPST436_23
23
23
23
OPST516_23
OPST526_23
OPST536_23
92
OPAZ530
OPAZ531
REFERENCES
OPAZ510
OPAZ511
STD abutment
STD abutment
STD abutment
5.0
5.0
5.0
5.0
5.0
5.0
H 1.5/H 6
H 2.5/H 6
H 3.5/H 6
REFERENCES
3.4 H 4
3.4 H 6
OPSA304
OPSA306
4.0 H 4
4.0 H 6
OPSA404
OPSA406
5.0 H 4
5.0 H 6
OPSA504
OPSA506
6.0 H 4
6.0 H 6
OPSA604
OPSA606
REFERENCES
OPTT100
OPTT100-5
REFERENCES
3.4 H 4
3.4 H 6
OPPC304
OPPC306
4.0 H 4
4.0 H 6
OPPC404
OPPC406
5.0 H 4
5.0 H 6
OPPC504
OPPC506
6.0 H 4
6.0 H 6
OPPC604
OPPC606
93
REFERENCES
3.4 H 4
3.4 H 6
OPCA304
OPCA306
4.0 H 4
4.0 H 6
OPCA404
OPCA406
5.0 H 4
5.0 H 6
OPCA504
OPCA506
6.0 H 4
6.0 H 6
OPCA604
OPCA606
REFERENCES
94
PMMA
Base diameter 3.4 mm
Crown height 4 and 6 mm
MULT castable coping
MULT castable coping
3.4 H 4
3.4 H 6
OPCR304
OPCR306
4.0 H 4
4.0 H 6
OPCR404
OPCR406
5.0 H 4
5.0 H 6
OPCR504
OPCR506
6.0 H 4
6.0 H 6
OPCR604
OPCR606
REFERENCES
STERILE
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
0
0
0
0
0
OPMU0-0
OPMU0-1
OPMU0-2
OPMU0-3
OPMU0-4
H 1.5
H 2.5
H 3.5
H 0.75
H 1.5
H 2.5
H 3.5
18
18
18
30
30
30
30
OPMU18-1-IN
OPMU18-2-IN
OPMU18-3-IN
OPMU30-0-IN
OPMU30-1-IN
OPMU30-2-IN
OPMU30-3-IN
H 1.5
H 2.5
H 3.5
H 0.75
H 1.5
H 2.5
H 3.5
18
18
18
30
30
30
30
OPMU18-1
OPMU18-2
OPMU18-3
OPMU30-0
OPMU30-1
OPMU30-2
OPMU30-3
REFERENCES
STERILE
MUCAP
MUCAP-4
MUT100
MUT100-4
MUT200
MUT200-4
95
REFERENCES
MUC100
MUC200
MUC300
MUC400
MUA100
MUA100-4
MUA200
MUA200-4
REFERENCES
STERILE
96
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
0
0
0
0
0
OPMUN0-0
OPMUN0-1
OPMUN0-2
OPMUN0-3
OPMUN0-4
REFERENCES
STERILE
MUNCAP
MUNT100
MUNT100-4
MUNT200
MUNT200-4
MUNC100
MUNC200
MUNC300
MUNC400
MUNA100
MUNA100-4
MUNA200
REFERENCES
KITMUNPAC
MUNPAC100
MUNPAC110
PMMA
Narrow castable Pacific Multi-Unit
MUNPAC120
97
REFERENCES
STERILE
H 1.5
H 2.5
H 3.5
0
0
0
OPSC010
OPSC020
OPSC030
REFERENCES
Castable coping
4.0
OPSC100
Temporary coping
4.0
Protective cap
OPSC200
STERILE
4.0
OPSC300
4.0
OPSC410
OPSC500
OPSC500-4
OPSC600
OPSC600-4
4.0 (unitary)
4.0 (by 4)
PACIFIC SYSTEM
Full kit for Pacific prostheses
Medical Grade V Titanium
4.0
OPSC700
OPSC700-4
REFERENCES
KITOPSC800
OPSC800
98
PMMA
Castable coping
OPSC910
OPSC901
REFERENCES
STERILE
H 2.5
H 2.5
H 3.5
H 3.5
H 4.5
H 4.5
18
18
18
18
18
18
AR
AR
AR
AR
AR
AR
OPAC022
OPAC023
OPAC032
OPAC033
OPAC042
OPAC043
H 2.5
H 2.5
H 3.5
H 3.5
H 4.5
H 4.5
18
18
18
18
18
18
R
R
R
R
R
R
OPACR22
OPACR23
OPACR32
OPACR33
OPACR42
OPACR43
REFERENCES
Castable coping
4.8
OPAC100
Temporary coping
4.8
Protective cap
Medical grade V titanium
Protective cap
OPAC200
STERILE
4.8
OPAC300
4.8
OPAC410
OPAC500
OPAC500-4
OPAC600
OPAC600-4
4.8 (unitary)
4.8 (par 4)
OPAC700
OPAC700-4
99
REFERENCES
LOCATOR ABUTMENTS
Medical grade V titanium
Base diameter 4.0 mm
LOCATOR abutment
LOCATOR abutment
LOCATOR abutment
LOCATOR abutment
LOCATOR abutment
OPLA010
OPLA020
OPLA030
OPLA040
OPLA050
H 1.5
H 2.5
H 3.5
H 4.5
H 5.5
REFERENCES
OPLA100
Ref. 8524
OPLA200
Ref. 8527
OPLA300
Ref. 8529
OPLA400
OPLA700
Ref. 8558
OPLA710
Ref. 8548
OPLA720
Ref. 8915
OPLA730
Ref. 8547
OPLA740
Transfert LOCATOR
Aluminium Medical Grade
LOCATOR transfer (by 4)
Ref. 8505
OPLA500
Ref. 8530
OPLA600
Analog LOCATOR
Aluminium Medical Grade
LOCATOR analog 4 mm (by 4)
100
REFERENCES
INMHECV
INMHELV
INMHEXLV
INCHECV
INCHELV
INCHEXLV
OPMP250
OPCP160
Multi-Unit mandrel
MUM100
MUM100L
Multi-Unit wrench
Used for the screwing Axiom Multi-Unit straight abutment
Medical grade stainless steel
Multi-Unit wrench
MUW100
MUWS
Ref. 8913
OPML230
Ref. 8260
OPCL150
Ref. 8393
OPCL3E1
101
REFERENCES
Gripping tool
INCCD
OPCF100
Abutment Extractor-Gripper
Usable with aesthetic, standard and temporary abutment
Flexibase and custom SIMEDA implants, in titanium.
Medical Grade V Titanium
Short Extractor-Gripper
Long Extractor-Gripper
PROSTHESIS KITS
Prosthesis kit
INEXPS
INEXPL
REFERENCES
INMODOPP
Contain:
1 dynamometrical prosthetic wrench
1 wrench and 1 Multi-Unit mandrel
1 wrench and 1 short hexagonal mandrel
1 wrench and 1 long hexagonal mandrel
Empty prosthesis kit
INMODOPPV
Including:
1 wrench and 1 Multi-Unit mandrel
One 3/4 and one 1/4 grey inserts
KITMUOPP
102
INMODOPSAKV
REFERENCES
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
0
0
0
0
0
OPSF006
OPSF016
OPSF026
OPSF036
OPSF046
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
7
7
7
7
7
OPAF00-7
OPAF01-7
OPAF02-7
OPAF03-7
OPAF04-7
Try-in abutments
Try-in abutments
Try-in abutments
Try-in abutments
Try-in abutments
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
15
15
15
15
15
OPAF001
OPAF011
OPAF021
OPAF031
OPAF041
Try-in abutments
Try-in abutments
Try-in abutments
Try-in abutments
Try-in abutments
H 0.75
H 1.5
H 2.5
H 3.5
H 4.5
23
23
23
23
23
OPAF002
OPAF012
OPAF022
OPAF032
OPAF042
R
R
R
AR
AR
AR
H 2.5
H 3.5
H 4.5
H 2.5
H 3.5
H 4.5
18
18
18
18
18
18
OPCFR22
OPCFR32
OPCFR42
OPCF022
OPCF032
OPCF042
H 2.5
H 3.5
H 4.5
H 2.5
H 3.5
H 4.5
30
30
30
30
30
30
OPCFR23
OPCFR33
OPCFR43
OPCF023
OPCF033
OPCF043
103
D. RE-WORKING KIT
BROKEN SCREW EXTRACTION KIT
REFERENCES
OPKITRET
REFERENCES
INKITEXPR
REFERENCES
INMDS
INMDL
In the event of a problem with an implant, please contact Anthogyrs marketing department and we will provide you with
the best repair solution for your situation; moreover, a repair protocol is delivered with each alteration kit.
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AXIOMR-PX_NOT_GB 2015-10
Photos credits: Anthogyr - All rights reserved - Not contractual photos
Anthogy SAS
2 237, Avenue Andr Lasquin
74700 Sallanches - France
Phone +33 (0)4 50 58 02 37
Fax +33 (0)4 50 93 78 60
www.anthogyr.fr