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Titanium Coxial Forcep Dsek
EUDAMEDClass I (EU MDR)
Ref D50-3839.5Model D50-1040-9990
Identity
- Trade Name
- TITANIUM COXIAL FORCEP DSEK EUDAMED
- Device Name
- Ophthalmic Forceps EUDAMED
- Model / Reference
- D50-1040-9990 EUDAMEDD50-3839.5 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +G006D50383950N EUDAMED
- Basic UDI-DI
- ++G006OphthalmicForceps9B EUDAMED
- EMDN Code
- L03130401 TISSUE AND ORGAN GRASPING FORCEPS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Spain 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
Titanium Coxial Forcep Dsek by Daud Jee Mfg. Co — 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 | ++G006OphthalmicForceps9B | Class I | Active |
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Manufacturer
- Manufacturer
- Daud Jee Mfg. Co
- EUDAMED SRN
- PK-MF-000009615
- Authorised Representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Sources (1)
- EUDAMED e094dcbd-4a73-40ca-a349-bc38d8e5dd54 61 fields · synced Jul 17, 2026