Identity
- Trade Name
- ExactEtch FDA UDI
- Generic Name
- Ophthalmic knife, single-use FDA UDI
- Device Name
- ExactEtch MVR Knife, 20 Gauge, Angled FDA UDI
- Model / Reference
- 2700K FDA UDI
- Description
- ExactEtch MVR Knife, 20 Gauge, Angled FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00813059010995 FDA UDI
- FDA Product Code
- HNN FDA UDI
- GMDN Term
- Ophthalmic knife, single-use 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ophthalmic knife, single-use
ExactEtch by Diamatrix — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic knife, single-use.
- MANI Ophthalmic Knife — MANI, INC. · Class I
- Ophthalmic Knife — Katena Products, Inc. · Class I
- MANI Ophthalmic Knife — MANI, INC. · Class I
- MANI Ophthalmic Knife — MANI, INC. · Class I
- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- MANI Ophthalmic Knife — MANI, INC. · Class I
- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
- MANI Ophthalmic Knife — MANI, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Diamatrix
Sources (1)
- FDA UDI 999f164e-7398-4861-8555-1fb2a2d28d88 33 fields · synced Jun 6, 2026