This document specifies the requirements for information supplied by the manufacturer for a medical device or by the manufacturer for an accessory. 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.
![](https://cecr.co.in/wp-content/uploads/2024/06/medical-device-labelling-300x300.jpg)
![](https://cecr.co.in/wp-content/uploads/2024/06/medical-device-labelling-300x300.jpg)