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OENORM EN 45502-1
Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer
Edition
1998-10-01
OENORM EN 3475-703
Aerospace series - Cables, electrical, aircraft use - Test methods - Part 703: Permanence of manufacturer's marking
Edition
2002-10-01
OENORM EN 13857-3
Explosives for civil uses - Part 3: Information to be provided by the manufacturer or his authorised representative to the user
Edition
2003-02-01
OENORM EN 15085-2
Railway applications - Welding of railway vehicles and components - Part 2: Requirements for welding manufacturer
Edition
2024-03-01
ISO 15223-1 DAM 1
Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and Modified EC REP symbol to not be country or region specific
Edition
2024-05
ASD-STAN prEN 3512
Steel FE-PL1801 (100Cr6) - Vacuum induction melted and consumable electrode remelted - Hardened and tempered - Hollow bars for the manufacturer of bearings - 3,5 mm ≤ a ≤ 55mm
Edition
1999-03-31
BS EN ISO 14922
Thermal spraying. Quality requirements for manufacturers of thermal sprayed coatings
Edition
2021-11-01
PD CEN ISO/TR 20416
Medical devices. Post-market surveillance for manufacturers
Edition
2020-08-19
OENORM EN ISO 18113-3
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/DIS 18113-3:2021)
Edition
2021-09-01
OENORM EN ISO 18113-1
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO/DIS 18113-1:2021)
Edition
2021-09-01
