EU → North America Device Access

ProMove UK Ltd

GB-MF-000024808 · United Kingdom · Solihull

ProMove UK Ltd is registered in the European database on medical devices as a manufacturer, with 30 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa30

Authorised representative in the Union: Advena Limited.

Devices declared under this manufacturer

Showing 12 of 30 declared devices.

Catalogue references include BS, BUGG, CH1HS, CKIT2, CS, EVKIT.

European nomenclature codes declared: V0805038002, V0880.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED30
Country of registrationUnited Kingdom

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN30
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. ProMove UK Ltd was not found in either the U.S. or the Canadian register.

Other manufacturers in United Kingdom

All United Kingdom manufacturers →