← Back to catalogue
Disposable Biopsy Forceps
EUDAMEDClass IIa (EU MDR)
Ref EN ISO 13485:2016Model KLF-AΦ2.3×1000-BD
Identity
- Trade Name
- Disposable Biopsy Forceps EUDAMED
- Device Name
- Disposable Biopsy Forceps EUDAMED
- Model / Reference
- KLF-AΦ2.3×1000-BD EUDAMEDEN ISO 13485:2016 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 16942599807114 EUDAMED
- Basic UDI-DI
- B-16942599807114 EUDAMED
- EMDN Code
- L03130402 FORCEPS FOR EXTERNAL BODIES, REUSABLE EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Türkiye EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Disposable Biopsy Forceps by Hangzhou Kangsheng Medical Equipment Co., Ltd — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-16942599807114 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hangzhou Kangsheng Medical Equipment Co., Ltd
- EUDAMED SRN
- CN-MF-000049095
- Authorised Representative
- MedPath GmbH DE-AR-000000087
Sources (1)
- EUDAMED 875d80a0-5329-4c62-9121-0a9e90522f05 61 fields · synced Jun 18, 2026