Act Now to be Ready on Time – Guide to New Classification Rules for In Vitro Diagnostic Medical Devices
Continuing our series of publications, we outline the key changes to the classification of in vitro diagnostic medical devices in advance of the In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR) becoming fully applicable on 26 May 2022.

 

In advance of the In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (the IVDR) becoming fully applicable on 26 May 2022, we outline the key changes to the classification of in vitro diagnostic medical devices (IVDs).

In this briefing we cover:

  • Classes of IVDs 
  • Classification Rules 
  • Impact of Classification Changes 
  • Device Identification

Click here or on the image below to download our full briefing. 

Act Now to be Ready on Time – Guide to New Classification Rules for In Vitro Diagnostic Medical Devices.

 

Contributed by Laura Casey 

Key Contacts

Charleen O’Keeffe Senior Associate

Laura Scott Partner

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