Identity
- Trade Name
- Gemini diss /ligture forceps ,S/S EUDAMED
- Device Name
- Gemini diss /ligture forceps ,S/S EUDAMED
- Model / Reference
- 1243120 EUDAMED
Identifiers
- Primary DI / UDI-DI
- G47212431200 EUDAMED
- Basic UDI-DI
- ++G4721243120RP EUDAMED
- EMDN Code
- L031310 DISSECTION FORCEPS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
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
Gemini diss /ligture forceps , S/S by HB Meditech (Pvt) Limited — 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 | ++G4721243120RP | Class I | Active |
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Manufacturer
- Manufacturer
- HB Meditech (Pvt) Limited
- EUDAMED SRN
- PK-MF-000024590
- Authorised Representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Sources (1)
- EUDAMED 34ca551b-185e-44c9-b2d8-a64e597970b7 61 fields · synced Jun 19, 2026