G-FLEX FLEXIBLE INSTRUMENTS EUROPE
BE-MF-000000623 · Belgium · Nivelles
G-FLEX FLEXIBLE INSTRUMENTS EUROPE is registered in the European database on medical devices as a manufacturer, with 119 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 119 |
|---|
Among these devices, 43 are declared sterile, 41 reusable.
Devices declared under this manufacturer
- Bite Block
- Cleaning Brush
- Endoscope Valves Set
- Inflation Devices
- Lithotripsy System
- Multiband Ligator
- Non-Sterile Reusable Biopsy Forceps
- Non-Sterile Reusable Foreign Body Retrievers
- Polyp Trap
- Sterile Disposable Biopsy Forceps
- Sterile Disposable Endoscopic Forceps & Retrievers
- Sterile Extraction Basket
Showing 12 of 119 declared devices.
Catalogue references include GF-OVL100-RU, GF-OVL501, GF230P-E, GF252203-25, GF4904, INFL40.
European nomenclature codes declared: G030799, G03050199, G0380, G0308010101, G0305010201, G03080399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 119 |
| 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 | 119 |
|---|---|
| Found in the U.S. device database | 17 |
| Share | 14.3 % |
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. G-FLEX FLEXIBLE INSTRUMENTS EUROPE was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
BE25/00000030 | supplemented | 2030-01-29 |