WILDmedical GmbH
DE-MF-000017096 · Germany · Tuttlingen
WILDmedical GmbH is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: MW01.204.15, MW08.200.04, MW08.502.01, MW08.530.13, MW16.350.09.
Among these devices, 14 are declared reusable.
Devices declared under this manufacturer
- DISSECTING Skalpell
- Drill
- Hand Held Drill
- Schraubendreher
Showing 12 of 14 declared devices.
Catalogue references include MW01.203.00, MW01.204.15, MW01.204.20, MW08.502.01, MW08.530.13, MW16.350.09.
European nomenclature codes declared: L0916, L010701, L010101, L01040503, L090401, L0102.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | WILDmedical GmbH (DE) · FDA 3015451162 |
| Devices in EUDAMED | 14 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 14 |
|---|---|
| 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: United States only. WILDmedical GmbH is registered in the United States but was not found in the Canadian register.