EU → US Device Access

CliniMed Limited

GB-MF-000023784 · United Kingdom · Loudwater

CliniMed Limited is registered in the European database on medical devices as a manufacturer, with 62 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa62

Among these devices, 14 are declared sterile.

Authorised representative in the Union: MT-AR-000000234.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED62
Country of registrationUnited Kingdom
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.

Notified body certificates

CertificateStatusExpiry
GB23/00000102issued2028-02-27

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