EU → North America Device Access

Sheffmed Limited

GB-MF-000004158 · United Kingdom · Rotherham

Sheffmed Limited is registered in the European database on medical devices as a manufacturer, with 236 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa236

Most frequent device types declared: Forceps - Non- Sterile, Forceps - Reusable, Forceps - Sterile, Probes, Mirrors and Hooks - Sterile, Retractors - Non-Sterile.

Among these devices, 67 are declared sterile, 97 reusable.

Authorised representative in the Union: Advena Limited.

Devices declared under this manufacturer

Showing 12 of 236 declared devices.

Catalogue references include E11-245, LAPBP0002, LAPFT0003, N20-100, P20-400ST, P60-401.

European nomenclature codes declared: Q0399, Q030499, Q030399, L149004, R9099, Q030199.

United States market access

FDA establishment registerRegistered with FDA
Matched entrySHEFFMED LIMITED (GB) · FDA 3003836856
Devices in EUDAMED236
Country of registrationUnited Kingdom

Device-level evidence

Devices with a numeric GTIN236
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: United States only. Sheffmed Limited is registered in the United States but was not found in the Canadian register.

Other manufacturers in United Kingdom

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