TIGGES-Zours GmbH
DE-MF-000008632 · Germany · Hattingen
TIGGES-Zours GmbH is registered in the European database on medical devices as a manufacturer, with 1 757 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 757 |
|---|
Devices declared under this manufacturer
- AB-Set TIGGES-Bandage zur TLO
- LWS-Miederoberteil
- OZO-Lumbalbandage TP
- T-FLEX B basic Überbrückungsorthese
- T-FLEX B basic Überbrückungsorthese, tailliert
- T-FLEX Flexionsorthese
- T-FLEX RSK Rahmenstützkorsett, tailliert
- T-FLEX Rekli Reklinationsorthese, tailliert
- T-FLEX TL Thorako-Lumbalorthese
- T-FLEX TL Thorako-Lumbalorthese, hoch
- TIGGES-Dorso basic BWS/LWS-Orthese
- TIGGES-Wirbelsäulenbandage M
Showing 12 of 1 757 declared devices.
Catalogue references include 01706-140weiß, 53919-125haut, 61239-140haut, 63339-135haut, 82109-75haut, 83339-120haut.
European nomenclature codes declared: Y060308, Y060309, Y060380, Y060307, Y06120601, Y061209.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 757 |
| 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 | 1 757 |
|---|---|
| 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. TIGGES-Zours GmbH was not found in either the U.S. or the Canadian register.