Identity
- Trade Name
- Diamatrix Ltd FDA UDI
- Generic Name
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- Kershner Capsulorrhexis Forceps, Thin Triangular Grasping tips, Angled 8mm from bend to tip, Diamond knurled handle with Flat, Guide pin stop for tip alignment, 102mm total length, Titanium FDA UDI
- Model / Reference
- F645T FDA UDI
- Description
- Kershner Capsulorrhexis Forceps, Thin Triangular Grasping tips, Angled 8mm from bend to tip, Diamond knurled handle with Flat, Guide pin stop for tip alignment, 102mm total length, Titanium FDA UDI
Identifiers
- Catalog Number
- F645T FDA UDI
- Primary DI / UDI-DI
- 00813059018243 FDA UDI
- FDA Product Code
- HNR FDA UDI
- GMDN Term
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Diamatrix Ltd by Diamatrix — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Diamatrix
Sources (1)
- FDA UDI 7e83715e-dcb1-41a1-8124-b5fdf3ec6df5 34 fields · synced May 30, 2026