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OENORM EN ISO 19001
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
Edition
2013-12-15
OEVE/OENORM EN ISO 15223-1
Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021)
Edition
2022-01-01
OEVE EN 160100
Sectional Specification: Capability approval of manufacturers of printed board assemblies of assessed quality
Edition
1998-01-14
BS EN ISO 17782
Petroleum, petrochemical and natural gas industries. Scheme for conformity assessment of manufacturers of special materials
Edition
2018-12-04
NF A91-223 ; NF EN ISO 14922:2021-10-06
Thermal spraying - Quality requirements for manufacturers of thermal sprayed coatings
Edition
2021-10-06
FD S99-125 ; FD CEN ISO/TR 20416:2020-09-23
Medical devices - Post-market surveillance for manufacturers
Edition
2020-09-23
OENORM EN ISO 18113-4
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO/DIS 18113-4:2021)
Edition
2021-09-01
OENORM EN ISO 18113-5
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/DIS 18113-5:2021)
Edition
2021-09-01
OENORM EN ISO 17664-1
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
Edition
2021-12-01
OENORM EN ISO 17664-2
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021)
Edition
2024-08-01