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OENORM EN 868-4
Packaging for terminally sterilized medical devices - Part 4: Paper bags - Requirements and test methods
Edition
2024-05-01
OENORM EN 868-2
Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
Edition
2024-05-01
OENORM EN ISO 10993-14
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
Edition
2009-09-15
OENORM EN ISO 10993-3
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)
Edition
2015-01-01
OENORM EN ISO 13408-7
Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012)
Edition
2015-11-15
OENORM EN ISO 10993-4
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)
Edition
2018-01-01
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
OENORM EN ISO 10993-15
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2019)
Edition
2023-08-15