EU → US Device Access

Endoscope-i Ltd

UK-MF-000044880 · United Kingdom · Birmingham

Endoscope-i Ltd is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa35

Most frequent device types declared: AGS – PL100.

Among these devices, 1 are declared active.

Authorised representative in the Union: PT-AR-000037982.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED35
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.

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