Identity
- Trade Name
- Single Use Foreign Body Forceps EUDAMED
- Device Name
- Single Use Foreign Body Forceps EUDAMED
- Model / Reference
- FBB12 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06926839810600 EUDAMED
- Basic UDI-DI
- 692683981s014S6 EUDAMED
- Direct Marketing DI
- 06926839810600 EUDAMED
- EMDN Code
- G03080199 GASTROINTESTINAL ENDOSCOPY, FORCEPS, SINGLE-USE - OTHER EUDAMED
Classification
- Device Class
- Class I 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 Foreign Body Forceps by Anrei Medical (HZ) 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 | 692683981s014S6 | Class I | Active |
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Manufacturer
- Manufacturer
- Anrei Medical (HZ) Co., Ltd.
- EUDAMED SRN
- CN-MF-000009964
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED 070708bd-87fd-4ada-93f2-94311b575233 61 fields · synced Jun 20, 2026