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OENORM EN ISO 10993-17
Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)
Edition
2024-02-15
OEVE/OENORM EN 62563-1
Medical electrical equipment - Medical image display systems - Part 1: Evaluation methods (IEC 62563-1:2009) (german version)
Edition
2014-08-01
OENORM EN 16872
Services of Medical Doctors with additional qualification in Homeopathy (MDQH) - Requirements for health care provision by Medical Doctors with additional qualification in Homeopathy
Edition
2017-04-15
UNE-EN ISO 9241-394
Ergonomics of human-system interaction - Part 394: Ergonomic requirements for reducing undesirable biomedical effects of visually induced motion sickness during watching electronic images (ISO 9241-394:2020) (Endorsed by Asociación Española de Normalización in May of 2022.)
Edition
2022-05-01
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
ONR 112005
Colour coding for medical gases
Edition
2010-07-01
ONR 112040
Selection of reprocessable medical devices
Edition
2012-04-01
ISO 3180
Fine ceramics (advanced ceramics, advanced technical ceramics) - Methods for chemical analysis of calcium-phosphate-based powders for non-biomedical applications
Edition
2023-07
ISO 4631
Corrosion of metals and alloys - Measurement of the electrochemical critical localized corrosion potential (E-CLCP) for Ti alloys fabricated via additive manufacturing method in simulated biomedical solutions
Edition
2023-11
PR NF S97-414
Restoration to suitable condition for use of medical devices for individual use - General requirements and safety