Carl Martin GmbH
DE-MF-000005066 · Germany · Solingen
Carl Martin GmbH is registered in the European database on medical devices as a manufacturer, with 3 594 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 3 594 |
|---|
Among these devices, 1 823 are declared reusable.
Catalogue references include 1162A/1, 1441, 1829, 400BU/2, 972/T2-T3-N, 973/CP2N.
European nomenclature codes declared: Q0199, L0399, L0901, L031399, Q010499, L010499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 3 594 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Carl Martin GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
HZ 1594091-1 | issued | 2026-06-29 |
HZ 1594091-1 | reissued | 2031-06-29 |