Single Use Biopsy Forceps
by Zhejiang Chuangxiang Medical Technology Co., LTD. 257 variants
Ref MD-H-BF1112
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number697040181BFHNECoatHM | Date8 Feb 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / reference
- MD-H-BF1112
- Primary DI / UDI-DI
- 06936534334721, 06936534333465
- Basic UDI-DI
- 697040181BFHNECoatHM
- EMDN code
- G0308010101 Gastrointestinal endoscopy, cold biopsy forceps, single-use
- Device class
- Class IIa
- EU registration type
- Standard device
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- CN-MF-000012417
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Zhejiang Chuangxiang Medical Technology Co., Ltd.
See all devices from Zhejiang Chuangxiang Medical Technology Co., Ltd. →
Properties
Other properties (13)
- Sterilise before use: No
- Implantable: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No