Identity
- Trade Name
- Bausch + Lomb FDA UDI
- Generic Name
- Ophthalmic laser system beam guide FDA UDI
- Device Name
- 23G STD L PROBE C 5/BOX FDA UDI
- Model / Reference
- BL5293C FDA UDI
- Description
- 23G STD L PROBE C 5/BOX FDA UDI
Identifiers
- Catalog Number
- BL5293C FDA UDI
- Primary DI / UDI-DI
- 10757770507655 FDA UDI
- 510(k) Number
- K122905 FDA UDI
- FDA Product Code
- HQB FDA UDI
- GMDN Term
- Ophthalmic laser system beam guide FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4690 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
No
FDA UDI
Category: Ophthalmic laser system beam guide
Bausch + Lomb by Bausch & Lomb Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K122905 also covers:
- Bausch + Lomb — Bausch & Lomb Incorporated
- Bausch + Lomb — Bausch & Lomb Incorporated
- Bausch + Lomb — Bausch & Lomb Incorporated
- Bausch + Lomb — Bausch & Lomb Incorporated
- Bausch + Lomb — Bausch & Lomb Incorporated
- 27GA Curved Laser Probe — Peregrine Surgical, LLC.
- 27GA Curved Laser Probe - Iridex — Peregrine Surgical, LLC.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bausch & Lomb Incorporated
Sources (1)
- FDA UDI 7bd521f3-75c4-4b2a-9838-036a555d0946 35 fields · synced Jun 8, 2026