Identity
- Trade Name
- Revital-Ox Resert FDA UDI
- Generic Name
- Medical device disinfection solution test strip FDA UDI
- Device Name
- The Revital-Ox Resert R60 Solution Test Strip is a chemical indicator designed exclusively for monitoring of Revital-Ox RESERT High Level Solutions. FDA UDI
- Model / Reference
- PCC054 FDA UDI
- Description
- The Revital-Ox Resert R60 Solution Test Strip is a chemical indicator designed exclusively for monitoring of Revital-Ox RESERT High Level Solutions. FDA UDI
Identifiers
- Catalog Number
- PCC054 FDA UDI
- Primary DI / UDI-DI
- 10724995002227 FDA UDI
- FDA Product Code
- JOJ FDA UDI
- GMDN Term
- Medical device disinfection solution test strip FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2800 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
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
Revital-Ox Resert by Albert Browne , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Albert Browne , Ltd.
Sources (1)
- FDA UDI 0d359eb6-d91b-4df9-8fb8-3cc8a0f9c0f0 37 fields · synced May 29, 2026