Identity
- Trade Name
- OMNIGUIDE BeamPath OTO-U Fiber FDA UDI
- Generic Name
- Ophthalmic laser system beam guide FDA UDI
- Device Name
- Laser Fiber FDA UDI
- Model / Reference
- OTO-U FDA UDI
- Description
- Laser Fiber FDA UDI
Identifiers
- Catalog Number
- OTO-U FDA UDI
- Primary DI / UDI-DI
- 00852306007753 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- Ophthalmic laser system beam guide FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Ophthalmic laser system beam guide
OMNIGUIDE BeamPath OTO-U Fiber by Omniguide, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Omniguide, Inc.
Sources (1)
- FDA UDI 81e2434e-7772-4abc-991d-9d2946ec3b13 34 fields · synced Jun 8, 2026