Guidance Document - Private Label Medical Devices

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Medical Devices Guidance Documents, Health And Safety

Published

December 7, 2004

Last updated

March 15, 2011

Description

2005 (revised 2011) Health Canada document providing guidance on regulatory requirements for private label manufacturers of Class II, III and IV medical devices

Organization

Country / Region

Canada

License

Open Government License 2.0 (Canada)

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