Preconditions
General:
- Quality Management certified according to DIN EN ISO 9001:2008
- Pressure Equipment Directive 97/23/EC (DGRL)
Welding:
- Welder’s certificate: EN 729-2 / AD2000 HPO
- Verification of all welding procedures: EN 288-3 / AD2000 HP2/1 / 97/23/EC
- Welding supervision: EN 719
- Welder tested according to the DGRL: EN 287-1 / AD2000 HP3
- Machine operator tested according to the DGRL: EN 1418 / AD2000 HP3
- Marking-transfer agreement with the TÜV- Nord
- Certified inspectors according to EN 473 for endoscopy (VT), dye penetrant test and evaluation of radiographies (RT1, RT2, FAS)
Documentation:
- According to Pressure Equipment Directive with operating instruction 97/23/EC Art. 3 Para. 3 (standard)
- From Category 1 with CE Marking
- Models, drawings, and part lists using the CAE-System
- Goods intake documentation to be checked against the specification of the order
- Manufacture-related documentation (material, surface finish, dimensional accuracy)
- Weld documentation with as-built one-line isometry, recorded weld parameters, and endoscopy
Factory Acceptance Test:
- Final test carried out by our Quality Assurance Department (standard)
- Final test according to the Pressure Equipment Directive (or by specified institution)
- Functional wet test run according to the customer's requirements
- Endoscopy with photo/video documentation
- X-ray radioscopic examination
- Riboflavin test for CIP capability
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