RENOL
BE-MF-000000785 · Belgium · Hélécine
RENOL is registered in the European database on medical devices as a manufacturer, with 150 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 150 |
|---|
Devices declared under this manufacturer
- Ambulation Ankle Holders Medium
- Crisis Bag Complete Small/Medium
- Extender nylon strap
- Pelvic Belt
- Roll Belt Small/Medium
- Roll Belt with 2 side straps Large + Pelvic
- Roll Belt with 2 side straps Small/Medium
- Security Wrist Holders Medium
- Standard Ankle Holders Large
- Standard Wrist Holders Medium
- Waist + Shoulder + Pelvic Belt
- Waist Safety Lock Belt Large
Showing 12 of 150 declared devices.
Catalogue references include RFA17220, RFA17400RL, RFB10115M, RFC47115, RFC57140, RFS20050.
European nomenclature codes declared: V0804.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 150 |
| Country of registration | Belgium |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 150 |
|---|---|
| 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. RENOL was not found in either the U.S. or the Canadian register.