Titanium Bonn Corneal Forcep 0.12
FDA UDIEUDAMEDClass I (US FDA UDI)
Identity
- Trade Name
- TITANIUM BONN CORNEAL FORCEP 0.12 EUDAMEDFDA UDIBONN CORNEAL FORCEP 0.12 EUDAMEDFDA UDI
- Generic Name
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- Ophthalmic Forceps EUDAMEDThis instrument is used to grasp, retract, or stabilize tissue. FDA UDI
- Model / Reference
- DT50-5514 EUDAMEDFDA UDID50-5513 EUDAMEDFDA UDID50-1040-9990 EUDAMED
- Description
- This instrument is used to grasp, retract, or stabilize tissue. FDA UDI
Identifiers
- Catalog Number
- DT50-5514 FDA UDID50-5513 FDA UDI
- Primary DI / UDI-DI
- +G006D50551309 EUDAMED+G006DT5055140$ EUDAMEDG006DT5055140 FDA UDIG006D5055130 FDA UDI
- Basic UDI-DI
- ++G006OphthalmicForceps9B EUDAMED
- FDA Product Code
- HNR FDA UDI
- EMDN Code
- L03130401 TISSUE AND ORGAN GRASPING FORCEPS, REUSABLE 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
- Spain EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
Yes
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Titanium Bonn Corneal Forcep 0.12 by Daud Jee Mfg. Co — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Daud Jee Mfg. Co
Sources (4)
- FDA UDI 8e72fcc5-9d6a-4fd2-82f2-7a4b20136b6c 34 fields · synced Jul 20, 2026
- FDA UDI 36a53960-dded-414c-ae5f-0c0bf628cb8f 34 fields · synced May 30, 2026
- EUDAMED b8d46b6e-c801-4199-aa55-4bde531067f4 61 fields · synced Jul 15, 2026
- EUDAMED f1cd5ae5-ebc9-4e32-9a64-fb0589fe64b8 61 fields · synced Jul 20, 2026