Dornier MedTech GmbH
DE-MF-000009774 · Germany · Weßling
Dornier MedTech GmbH is registered in the European database on medical devices as a manufacturer, with 65 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 64 |
|---|---|
| Class IIa | 1 |
Among these devices, 65 are declared active.
Devices declared under this manufacturer
- Dornier Aries 2
- Dornier Compact Sigma
- Dornier Delta III
- Dornier Delta III Pro
- Dornier H100
- Dornier H140
- Dornier HRM
- Dornier Medilas H100
- Dornier Medilas H140
- Dornier Relax + Endo
- Dornier Solvo H30
- Dornier Thulio
Showing 12 of 65 declared devices.
Catalogue references include K1025661, K1045936, K1047468, K2011210, K2011730, K2014700.
European nomenclature codes declared: Z12020301, Z12030201, Z12011003, Z12011016, Z12160101, Z12139001.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | DORNIER MEDTECH GMBH (DE) · FDA 9611388 |
| Devices in EUDAMED | 65 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 54 |
|---|---|
| Found in the U.S. device database | 6 |
| Share | 11.1 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | DORNIER MEDTECH GMBH |
North American profile: Both markets. Dornier MedTech GmbH is registered in both the United States and Canada.