Identity
- Trade Name
- Capsulorhexis forceps- Non Sterile EUDAMEDMASKET CAPSULORRHEXIS FCPS FDA UDI
- Generic Name
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- Capsulorhexis forceps- Non Sterile EUDAMEDThis instrument is used to grasp, retract, or stabilize tissue. FDA UDI
- Model / Reference
- D50-5084 EUDAMEDFDA UDI
- Description
- This instrument is used to grasp, retract, or stabilize tissue. FDA UDI
Identifiers
- Catalog Number
- D50-5084 FDA UDI
- Primary DI / UDI-DI
- G006D505084 EUDAMEDG006D5050840 FDA UDI
- Basic UDI-DI
- ++G006D505084VW EUDAMED
- FDA Product Code
- HNR FDA UDI
- EMDN Code
- L03130499 GRASPING FORCEPS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Capsulorhexis forceps- Non Sterile by Daud Jee Mfg. Co — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++G006D505084VW | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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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 (2)
- EUDAMED dee8c4e5-7c3c-4dc7-b988-f980a70c2980 61 fields · synced Jun 18, 2026
- FDA UDI d1107354-345c-424c-92e5-bc6ec8ab378a 34 fields · synced May 30, 2026