Identity
- Trade Name
- OXYSEPT FDA UDI
- Generic Name
- Contact lens protein-removal solution FDA UDI
- Device Name
- OXYSEPT (ULTRACARE) 12OZ + 36 TABLETS FDA UDI
- Model / Reference
- 93002 FDA UDI
- Description
- OXYSEPT (ULTRACARE) 12OZ + 36 TABLETS FDA UDI
Identifiers
- Catalog Number
- 93002 FDA UDI
- Primary DI / UDI-DI
- 00827444000140 FDA UDI
- FDA Product Code
- LPN FDA UDI
- GMDN Term
- Contact lens protein-removal 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
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
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: Contact lens protein-removal solutionSoft contact lens cleaning solution
Oxysept by Johnson & Johnson Surgical Vision, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Soft contact lens cleaning solution.
- Bausch + Lomb — Bausch & Lomb Incorporated · 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
- Johnson & Johnson Surgical Vision, Inc.
Sources (1)
- FDA UDI 55bc3dd5-a5a0-4e77-afbf-bdc3264b876e 35 fields · synced Jun 9, 2026