90.92 Standard to be revised Dec 18, 2023
ISO
ISO/TC 210 Quality management and corresponding general aspects for medical devices
International Standard
11.040.01 Medical equipment in general
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.
PUBLISHED
ISO 20417:2021
90.92
Standard to be revised
Dec 18, 2023
IN_DEVELOPMENT
ISO/DIS 20417