EU → North America 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: AidaCare-Hygieneüberzug für GRAF-Lagerungsschale, GRAF-Lagerungsschale inkl. GRAF-Führungsarm, RELEXTA Spreizwindel T1, RELEXTA-Abspreizwindel Typ I, Relexta-Abspreizhose Typ I.

Devices declared under this manufacturer

Showing 12 of 23 declared devices.

Catalogue references include 500-01, 600-10-T1, 600-12-T2, 600-16-T1, 700-02, 70507-SG.

European nomenclature codes declared: Y061215, V9099, T030102.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED23
Country of registrationGermany

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN22
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: Neither register. AIDAMED - Produktion & Vertrieb medizinische Produkte & Geräte was not found in either the U.S. or the Canadian register.

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