Renfert GmbH
DE-MF-000005448 · Germany · Hilzingen
Renfert 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: Sympro.
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- Drahtnetze fein 50x10cm vergoldet RL
- Drahtnetze mittel 50x10cm vergoldet RL
- Duomix II 230 V~, 50/60 Hz
- Dynamix ® speed 2
- SYMPRESS 230V, 50HZ
- SYMPRO 100-240 V~50/60Hz
- Sympress II 230 V~, 50/60 Hz
- Verstärkungsgitter 0,4mm vergoldet 5 Stk.
- Verstärkungsgitter 0,4mm 5 Stk.
- help:ex discolor f
- help:ex plaque f
- help:ex plaque p
Showing 12 of 14 declared devices.
Catalogue references include 2222100, 2350004, 2350104, 60000000, 66000000, 67000000.
European nomenclature codes declared: V0799, Q010699, Q010207.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | RENFERT GMBH (DE) · FDA 3001065024 |
| Devices in EUDAMED | 14 |
| Country of registration | Germany |
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. Renfert GmbH is registered in the United States but was not found in the Canadian register.