EU: Use of Symbols to Indicate Compliance with the Medical Devices Regulation

The Medical Devices Regulation 2017/745/EU (‘MDR’) has new requirements that ask for various kinds of information to be indicated on the label of medical devices. To comply with this requirement within the short term and in a harmonised manner, before the international standard is available, MedTech Europe publishes the present guidance on symbols for the following information.
1. Medical device
2. Contains human blood or plasma derivatives
3. Contains a medicinal substance
4. Contains hazardous substances
5. Contains biological material of human origin
6. Contains biological material of animal origin
7. Sterilized using vaporized hydrogen peroxide
8. Translation
9. Repackaging
10.  Single Patient Multiple us
Author(s)Source
MedTech EuropeMedTech Europe May 2019
This is a post of a scientific or business information. The information given here is checked thoroughly by “Implant-Register”. However we can´t be responsible for the content. Contact the publisher, if you have questions. You may inform us about changes of the information to improve the Register.
Comments: n/a
let us know
Scroll to Top