Technimed AG
CH-MF-000028263 · Switzerland · Rorschach
Technimed AG is registered in the European database on medical devices as a manufacturer, with 29 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 29 |
|---|
Most frequent device types declared: Secutape Grösse 2+.
Authorised representative in the Union: SGT Servicegesellschaft Technipack mbH.
Devices declared under this manufacturer
- Secutape Fixier-Set, Hydrocolloid
- Secutape Fixier-Set, Vliesbasis
- Secutape Fixierhalter Hydrocolloid, für Set
- Secutape Klettbinder-Set Gross
- Secutape Klettbinder-Set klein Hydrocolloid
- Secutape Kopfhalter-Set ECMO
- Secutape Krokofix klein
- Secutape Nasal-Set Hydrocolloid
- Secutape Soft-Set
- Secutape Tracheofix Basic
- Secutape Tracheofix Comfort
- Secutape Unifix
Showing 12 of 29 declared devices.
Catalogue references include 8500400, 8500600, 8500890, 8500900, 8501130, 8501410.
European nomenclature codes declared: R01038099, M0599, M040701, M03030299, M040799, M040203,R01038099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 29 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 29 |
|---|---|
| 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. Technimed AG was not found in either the U.S. or the Canadian register.