Identity
- Trade Name
- Non-Sterile Reusable Biopsy Forceps EUDAMED
- Device Name
- Non-Sterile Reusable Biopsy Forceps EUDAMED
- Model / Reference
- GF180 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05420051303397 EUDAMED
- Basic UDI-DI
- 54200513-TF17-BBF-RU-6Q EUDAMED
- EMDN Code
- G030799 GASTROINTESTINAL ENDOSCOPY, DIAGNOSTIC DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Belgium EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
Yes
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Non-Sterile Reusable Biopsy Forceps by G-Flex Flexible Instruments Europe — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Manufacturer's product page: Disposable & Reusable Biopsy Forceps
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 54200513-TF17-BBF-RU-6Q | Class I | Active |
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Manufacturer
- Manufacturer
- G-Flex Flexible Instruments Europe
- EUDAMED SRN
- BE-MF-000000623
Sources (1)
- EUDAMED 3824d8de-b6b1-4de5-bf21-09f37fd58eaa 61 fields · synced Jul 25, 2026