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Disposable Biopsy Forceps
EUDAMEDClass IIa (EU MDR)
Ref EN ISO 13485:2016Model KLF-AΦ2.3×1000-BS
Identity
- Trade Name
- Disposable Biopsy Forceps EUDAMED
- Device Name
- Disposable Biopsy Forceps EUDAMED
- Model / Reference
- KLF-AΦ2.3×1000-BS EUDAMEDEN ISO 13485:2016 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 16942599807084 EUDAMED
- Basic UDI-DI
- B-16942599807084 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
Category: Bronchoscopic biopsy curette, rigid
Disposable Biopsy Forceps by Hangzhou Kangsheng Medical Equipment Co., Ltd — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
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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-16942599807084 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Hangzhou Kangsheng Medical Equipment Co., Ltd
- EUDAMED SRN
- CN-MF-000049095
- Authorised Representative
- MedPath GmbH DE-AR-000000087
Sources (1)
- EUDAMED 29bbe025-10ce-46ef-b52d-0bfae3d9ccf8 61 fields · synced Jun 19, 2026