Adverse incidents: in vitro diagnostic (IVD) blood glucose meters

Information

Type

Guidance

Regulated products

IVDMD, Medical Devices

Topics

Health And Social Care

Published

January 26, 2015

Last updated

December 30, 2020

Description

Device-specific guidance for manufacturers on reporting adverse incidents under the vigilance system

Organization

Country / Region

United Kingdom

License

Open Government Licence 2.0 (United Kingdom)

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