Identity
- Trade Name
- Ophthalmic Knife FDA UDI
- Generic Name
- Ophthalmic knife, reusable FDA UDI
- Device Name
- Diamond Knife 2.5/3.5 Angle Mount J Slot Handle FDA UDI
- Model / Reference
- DK2535AM3D FDA UDI
- Description
- Diamond Knife 2.5/3.5 Angle Mount J Slot Handle FDA UDI
Identifiers
- Primary DI / UDI-DI
- G223DK2535AM3D0 FDA UDI
- FDA Product Code
- HNN FDA UDI
- GMDN Term
- Ophthalmic knife, 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 knife, reusable
Ophthalmic Knife by Medetz Surgical Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Ophthalmic knife, reusable.
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- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
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
- Medetz Surgical Instruments
Sources (1)
- FDA UDI 9d82b8ab-a1eb-4635-b02f-c21432fe1ef5 34 fields · synced May 30, 2026