Non-Sterile Reusable Biopsy Forceps
by G-Flex Flexible Instruments Europe 23 variants
Ref GF160P
Active
CE MDR
Valid until
29 Jan 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberBE25/00000030 | Date21 Aug 2026 | StatusActive |
Certificates
- BE25/00000030 Active
Quality management system EU MDR
- Certifier
- SGS Belgium NV 1639
- Issued
- 21 Aug 2026
- Expires
- 29 Jan 2030
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- GF160P
- Primary DI / UDI-DI
- 05420051300914
- Basic UDI-DI
- 54200513-TF17-BBF-RU-6Q
- EMDN Code
- G030799 Gastrointestinal endoscopy, diagnostic devices - other
- Device Class
- Class I
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- BE-MF-000000623
From the manufacturer
Manufacturer's product page: Disposable & Reusable Biopsy Forceps
Other devices from G-Flex Flexible Instruments Europe
Properties
Other properties (11)
- Sterile: No
- Implantable: No
- Contains Latex: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No