NOTE 1 There is guidance or rationale for this Clause contained in Clause A.2.
This document specifies the requirements for information supplied by the manufacturer for a medical device or by the manufacturer for an accessory, as defined in 3.1. This document includes the generally applicable requirements for identification and labels on a medical device or accessory, the packaging, marking of a medical device or accessory, and accompanying information. This document does not specify the means by which the information is to be supplied.
NOTE 2 Some authorities having jurisdiction impose different requirements for the identification, marking and documentation of a medical device or accessory.
Specific requirements of medical device product standards or group standards take precedence over requirements of this document.
ОБЈАВЉЕН
ISO 20417:2021
ПРОЈЕКАТ
ISO 20417
60.00
Стандард у поступку објављивања
21. 2. 2026.
Медицинска средства – Информације које пружа произвођач
50.60 Завршетак поступка одобравања дефинитивног текста нацрта стандарда
Медицинска средства – Информације које пружа произвођач
50.60 Завршетак поступка одобравања дефинитивног текста нацрта стандарда