EU → US Device Access

Cobi Rehab A/S

DK-MF-000001370 · Denmark · Karlslunde

Cobi Rehab A/S is registered in the European database on medical devices as a manufacturer, with 207 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa207

Most frequent device types declared: 0305-101-000, 0230-055-045, 3002-9017-000, 0316-100-000, 0319-7001-000.

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED207
Country of registrationDenmark
⚠️ 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.

Other manufacturers in Denmark

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