Вы находитесь на странице: 1из 1

PRESS U R E E Q UIPM ENT D IRECT IVE

Category and Module Decision Flowchart - 2014/68/EU

Start Maximum allowable pressure


greater than 0.5 bar(g)?
YES
Equipment excluded from
PED: Art. 1.2?
NO
Determine type of
Pressure Equipment

NO YES
X, Y and Z are entry
points for pressure
accessories and/or PED does not apply PED does not apply
assemblies

VESSEL (FIRED) HEATED PIPING SAFETY ACCESSORIES PRESSURE ACCESSORIES ASSEMBLIES


PRESSURE EQUIPMENT

Go to
X Y
Determine state of Determine state of Manufactured for The volume is more Assemblies referred to in Article 4
appropriate than the YES point
fluid contents fluid contents specific equipment X (2) shall be subjected to a global
nominal size DN? conformity assessment
GAS LIQUID GAS LIQUID YES NO NO procedure comprising:

Determine fluid group* Determine fluid group* Determine fluid group* Determine fluid group* Classified The nominal size DN is more Go to Assessment of each item of
in the same appropriate than the volume?
YES point pressure equipment making
Group 1 Group 2 Group 1 Group 2 Group 1 Group 2 Group 1 Group 2 Choose a Y
category up the assembly and referred
module from
as the NO to in Article 4 (1) which has not
Category IV
Table 1* Table 3* Table 4* Table 5* Table 6* Table 7* Table 8* Table 9* equipment it been previously subjected to a
Table 2*
protects conformity assessment procedure
The nominal size DN
and the volume are and to a separate CE marking;
Determine maximum allowable pressure in bar Determine maximum allowable pressure in bar equally appropriate the assessment procedure shall
and volume in litres and nominal size DN in mm be determined by the category of
each item of equipment;
Use the table to determine the appropriate conformity assessment category Compare the output category,
starting from X, with that
from Y, and take the highest Assessment of the integration
Choose a module from the category or a higher category
Z category of these two of the various components
of the assembly as referred to in
sections 2.3, 2.8 and 2.9 of
SEP Annex I, which shall be determined
CATEGORY II CATEGORY III CATEGORY IV Go to by the highest category applicable
point
+ + +
SOUND MODULE B MODULE B MODULE B to the equipment concerned other
ENGINEERING MODULE A2 MODULE D MODULE C2 MODULE D Z
PRACTICE (DESIGN TYPE) (PRODUCTION TYPE) (PRODUCTION TYPE) than that applicable to any safety
accessories;
CATEGORY I MODULE D1 MODULE B
(DESIGN TYPE) + MODULE F MODULE B
(PRODUCTION TYPE) + MODULE E MODULE B
(PRODUCTION TYPE) + MODULE F
* Conformity assessment tables. To determine which
applies to your asset, use the Lloyd’s Register PED Assessment of the protection of
MODULE A MODULE E1 MODULE H MODULE G MODULE H1 category selection mobile or desktop app, found at an assembly against exceeding
www.lr.org/ped. When reviewing the tables, please the permissible operating limits
note the exceptions.
as referred to in sections 2.10 and
3.2.3 of Annex I, shall be conducted
in the light of the highest category
applicable to the items of
PED modules: Notified Body involvement summarised equipment to be protected.
Manufacturers may select from a range of conformity assessment modules to show the Essential Safety Requirements are met, which include: KEY TERMS

• Manufacturer’s self-certification Please note: The following are summaries of the Notified Body’s CoC – Certificate of Conformity Go to
• Third-party type examination or design examination involvement and are not exhaustive. To determine which applies to DoC – Declaration of Conformity point
• Third-party inspection your asset, use the Lloyd’s Register PED category selection desktop ESRs – Essential Safety Requirements Z
• Quality management system certification tool or our mobile app. Visit www.lr.org/ped for more information. NoBo – Notified Body

MODULE A MODULE A2 MODULE B MODULE B MODULE C2 MODULE D MODULE D1


Internal Production Control Internal Production Control plus random (PRODUCTION TYPE) (DESIGN TYPE) Conformity to type based on internal Conformity to type based on Production Production Quality Assurance
pressure equipment checks EU type examination – production type EU type examination – design type production control plus random pressure Quality Assurance
NOBO’S RESPONSIBILITY: equipment checks NOBO’S RESPONSIBILITY:
• None NOBO’S RESPONSIBILITY: NOBO’S RESPONSIBILITY: NOBO’S RESPONSIBILITY: NOBO’S RESPONSIBILITY: • Assess quality system, including
• Examine technical documentation • Examine technical documentation NOBO’S RESPONSIBILITY: • Assess quality system, including inspection visit inspection visit
• Monitor through unexpected visits
• Assess materials and check certificates • Assess materials • Carry out checks at random intervals to verify • Conduct surveillance visits to ensure • Conduct surveillance visits to ensure
• Ensure manufacturer performs final quality of final assessment and internal checks on
assessment according to Sec. 3.2 of ESRs • Approve procedures for permanent joining or • Approve procedures for permanent joining pressure equipment
manufacturer fulfils obligations from manufacturer fulfils obligations from
• Take samples of pressure equipment to check they have been previously approved or check they have been previously • Ensure manufacturer performs final assessment approved quality system approved quality system
• Verify the joining and NDE personnel are approved • Carry out periodic audits in such a frequency • Carry out periodic audits in such a
conduct checks according to Section 3.2 of ESRs
qualified or approved • Draw up evaluation report • Take samples of pressure equipment to conduct that a full reassessment is carried out every frequency that a full reassessment is
• Assess number to sample and whether it • Issue EU type-examination certificate -
is necessary to perform all or part of final • Carry out appropriate examinations and tests checks three years carried out every three years
design type • Assess number to sample and whether it
assessment on the samples to check if the chosen standards are applied • Carry out unexpected visits • Carry out unexpected visits
• Notify NoBo approving authority and other is necessary to perform all or part of final
correctly NoBos assessment on the samples • Assess proposed changes to the quality system • Assess proposed changes to the quality
• Draw up evaluation report • For category III and IV vessels for Group 1 and 2 system
• Issue EU type-examination certificate - gases and Group 1 liquids and steam generators,
production type take a sample of equipment and perform proof
• Notify NoBo approving authority and other NoBos test referred to in Section 3.2.2 of ESRs

MODULE E MODULE E1 MODULE F MODULE G MODULE H MODULE H1 MODULE SEP


Conformity based on Pressure Equipment Quality Assurance of Final Pressure Conformity based on Pressure Equipment Conformity based on Unit Verification Conformity based on Full Quality Conformity based on Full Quality Sound Engineering Practice
Quality Assurance Equipment inspection and testing Verification NOBO’S RESPONSIBILITY: Assurance Assurance plus design examination NOBO’S RESPONSIBILITY:
NOBO’S RESPONSIBILITY: NOBO’S RESPONSIBILITY: NOBO’S RESPONSIBILITY: • Examine design and construction of each item NOBO’S RESPONSIBILITY: NOBO’S RESPONSIBILITY: • None
• Assess quality system, including inspection • Assess quality system, including • Examine and test each item of pressure • Examine technical documentation with • Assess quality system, including inspection visit in addition to the requirements of Module H:
visit inspection visit equipment to verify each item conforms to the respect to design and manufacturing • Conduct surveillance visits to ensure • Issue an EC design-examination certificate
• Conduct surveillance visits to ensure • Conduct surveillance visits to ensure type and requirements of the Directive procedures manufacturer fulfils obligations from • Carry out increased surveillance of the final
manufacturer fulfils obligations from manufacturer fulfils obligations from • Verify the joining and NDE personnel are • Assess materials approved quality system assessment in the form of unexpected visits
approved quality system approved quality system qualified or approved • Verify material manufacturers’ certificates • Carry out periodic audits in such a frequency which must include examinations on the
• Carry out periodic audits in such a frequency • Carry out periodic audits in such a • Verify material manufacturers’ certificates • Approve procedures for permanent joining of that a full reassessment is carried out every pressure equipment
that a full reassessment is carried out every frequency that a full reassessment is parts or check previous approval three years • Assess any modifications to the approved
• Carry out or have carried out final inspection
three years carried out every three years • Carry out unexpected visits design and give additional approval
and proof test as referred to in Section 3.2 of • Verify the joining and NDE personnel are
• Carry out unexpected visits • Carry out unexpected visits the ESRs qualified or approved • Assess proposed changes to the quality system
• Assess proposed changes to the quality system • Assess proposed changes to the quality • Draw up written CoC for the tests carried out • Perform appropriate tests during manufacture • For category III vessels for Group 1 gases,
• For category III vessels for Group 1 gases, system • Carry out final inspection and perform or Group 2 gases and Group 1 liquids and steam
Group 2 gases and Group 1 liquids and steam have performed proof test as referred to in generators, take a sample of equipment and
generators, take a sample of equipment Section 3.2 of the ESRs perform or have performed the proof test
and perform the the proof test referred to in • Draw up CoC for the tests carried out referred to in Section 3.2.2 of the ESRs
Sec. 3.2.2 of the ESRs • For one-off production of category III steam
generators, the proof test must be performed
for each unit

To find out more about how Lloyd’s Register can help you, email inspection@lr.org
or visit www.lr.org

Lloyd’s Register assumes no responsibility and shall not be liable to any person for any loss, damage or expense
caused by reliance on the information or advice in this document or howsoever provided.
Lloyd’s Register, LR and any variants are trading names of Lloyd’s Register Group Limited, its subsidiaries and affiliates.
© Lloyd’s Register Group Limited 2018

Вам также может понравиться