Technologie Institut Medizin GmbH (TIM)
DE-MF-000018722 · Germany · Koblenz
Technologie Institut Medizin GmbH (TIM) is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 10 |
|---|---|
| Class IIa | 3 |
Among these devices, 10 are declared active.
Devices declared under this manufacturer
- CLEAN AIR®
- LISA
- MIRUS™ Controller
- SmartVap™
Showing 12 of 13 declared devices.
Catalogue references include MC-ISO, MC-SEVO, ML44-3, ORS-VAC, SV-DES-A-B, SV-DES-S-B.
European nomenclature codes declared: R9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| 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 | 13 |
|---|---|
| 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. Technologie Institut Medizin GmbH (TIM) was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
44911220469 | amended | 2028-11-28 |