EU → US Device Access

AIDAMED - Produktion & Vertrieb medizinische Produkte & Geräte

DE-MF-000008562 · Germany · Nürnberg

AIDAMED - Produktion & Vertrieb medizinische Produkte & Geräte 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: Relexta-Beuge-Spreizwindel T2, Relexta-Spreizwindel T1, RELEXTA-Abspreizwindel Typ I, GRAF-Lagerungsschale inkl. GRAF-Führungsarm, Relexta-Abspreizhose Typ I.

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 EUDAMED23
Country of registrationGermany
⚠️ 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 Germany

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