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DIN EN ISO 20417
Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021, Corrected version 2021-12); German version EN ISO 20417:2021
Edition
2022-03
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
OENORM EN 16570
Information technology - Notification of RFID - The information sign and additional information to be provided by operators of RFID application systems
Edition
2015-02-15
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/OENORM EN ISO 15223-1/A1
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 (ISO 15223 1:2021/DAM 1:2024)
Edition
2024-06-15
OEVE/OENORM EN ISO 20417
Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021, Corrected version 2021-12)
Edition
2022-09-01
SN 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
2021-10
SN 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
2021-10
SN 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
2024-01