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Reusable Biopsy Forceps
EUDAMEDClass I (EU MDR)
Ref AF-2423BSModel Reusable Biopsy Forceps
Identity
- Trade Name
- Reusable Biopsy Forceps EUDAMED
- Device Name
- Reusable Biopsy Forceps EUDAMED
- Model / Reference
- Reusable Biopsy Forceps EUDAMEDAF-2423BS EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06970671383488 EUDAMED
- Basic UDI-DI
- 697067138BT014E4 EUDAMED
- EMDN Code
- L031301 GENERAL SURGERY BIOPSY FORCEPS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
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
Reusable Biopsy Forceps by Alton (Shanghai) Medical Instruments Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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 | 697067138BT014E4 | Class I | Active |
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Manufacturer
- Manufacturer
- Alton (Shanghai) Medical Instruments Co., Ltd.
- EUDAMED SRN
- CN-MF-000012832
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED fffdb5c0-5066-42eb-9fe0-13f09f1822c0 61 fields · synced Jun 19, 2026