tic Medizintechnik GmbH
DE-MF-000033923 · Germany · Dorsten
tic Medizintechnik GmbH is registered in the European database on medical devices as a manufacturer, with 115 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 115 |
|---|
Most frequent device types declared: BASIC+LINE / SaneoLINE, Intracorporeal electrode for connection to electrical stimulation and , Newton / Kopernikus / Cassini, PRIMUSmed, PremiumLINE.
Among these devices, 19 are declared active, 5 with a measuring function.
Devices declared under this manufacturer
- SaneoONE
- femicare Bowl Pessary 90 mm
- femicare Cube Pessary 70 mm
- femicare Cube Pessary perforated 41 mm
- femicare Cube Pessary perforated 55 mm
- femicare Thick Ring Pessary 50 mm
- femicare Thick Ring Pessary 55 mm
- femicare Thick Ring Pessary 75 mm
- femicare Thick Ring Pessary 80 mm
- femicare Urethra Bowl Pessary 65 mm
- femicare Urethra Pessary 50 mm
- femicare Urethra Pessary 55 mm
Showing 12 of 115 declared devices.
Catalogue references include CP41, CP55, TR50, TR55, TR75, U55.
European nomenclature codes declared: U070399, Z12062799, U0780, N01028099, U0599, U99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 115 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 115 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
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. tic Medizintechnik GmbH was not found in either the U.S. or the Canadian register.