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GS Elektromedizinische Geräte G. Stemple GmbH

DE-MF-000007648 · Germany · Kaufering

GS Elektromedizinische Geräte G. Stemple GmbH is registered in the European database on medical devices as a manufacturer, with 63 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa54
Class IIb6
Class I3

Most frequent device types declared: 00002, 00007, 00009, 00011, 00013.

Among these devices, 21 are declared active, 3 with a measuring function.

Devices declared under this manufacturer

Showing 12 of 63 declared devices.

Catalogue references include 04120.21, 04120.821, 04222.0002, 04233.04, 05405.1, 09300.

European nomenclature codes declared: Z12030580, Z12050380, Z120304, Z12040180, Z11069001, Z12030599.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED63
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 GTIN63
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. GS Elektromedizinische Geräte G. Stemple GmbH was not found in either the U.S. or the Canadian register.

Other manufacturers in Germany

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