EU → North America Device Access

Mattana UK Limited

UK-MF-000050755 · United Kingdom · Hampshire

Mattana UK Limited is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa23

Most frequent device types declared: Post Op Breast Augmentation Band.

Authorised representative in the Union: AF Pharma Service Europe SL.

Devices declared under this manufacturer

Showing 12 of 23 declared devices.

Catalogue references include 850077907487, B07VV1S2PB, B07XXMGTNL, B0CG9LQKT5, B0CG9LQNFJ, B0FHQ74ZPW.

European nomenclature codes declared: M030499.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED23
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 GTIN23
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. Mattana UK Limited was not found in either the U.S. or the Canadian register.

Other manufacturers in United Kingdom

All United Kingdom manufacturers →