Identity
- Trade Name
- Bausch + Lomb FDA UDI
- Generic Name
- Soft contact lens cleaning solution FDA UDI
- Device Name
- Soft Contact Lens Cleaning Solution 1 FL OZ FDA UDI
- Model / Reference
- 621004 FDA UDI
- Description
- Soft Contact Lens Cleaning Solution 1 FL OZ FDA UDI
Identifiers
- Catalog Number
- FCP-4838 FDA UDI
- Primary DI / UDI-DI
- 00310119010044 FDA UDI
- FDA Product Code
- LPN FDA UDI
- GMDN Term
- Soft contact lens cleaning solution FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5928 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
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: Soft contact lens cleaning solution
Bausch + Lomb by Bausch & Lomb Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Soft contact lens cleaning solution.
- OXYSEPT — Johnson & Johnson Surgical Vision, Inc. · Class II
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
- Bausch & Lomb Incorporated
Sources (1)
- FDA UDI cf691c06-1dd7-402e-b42c-2f41a958dea5 34 fields · synced Jun 8, 2026