Identity
- Device Name
- Single-Use Biopsy Forceps EUDAMED
- Model / Reference
- 99 06 47 02 80 4 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06932619700122 EUDAMED
- Basic UDI-DI
- 69326197BF387119U EUDAMED
- EMDN Code
- G0308010101,R0702010101 EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
Single-Use Biopsy Forceps by Transmed (china) Co., Ltd. — Class IIa — 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 | 69326197BF387119U | Class IIa | Active |
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Manufacturer
- Manufacturer
- Transmed (China) Co., Ltd.
- EUDAMED SRN
- CN-MF-000029614
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED 8821ecf5-83b0-4ea5-9347-4f7ebe3bd4f2 61 fields · synced Jul 15, 2026