Identity
- Trade Name
- VERDOC FDA UDI
- Generic Name
- Chemical/physical sterilization process indicator FDA UDI
- Device Name
- The Verdoc Vaporized VH202 Record Card with process indicator is designed for use exclusively in the V-PRO Low Temperature Sterilization Systems. FDA UDI
- Model / Reference
- RK033 FDA UDI
- Description
- The Verdoc Vaporized VH202 Record Card with process indicator is designed for use exclusively in the V-PRO Low Temperature Sterilization Systems. FDA UDI
Identifiers
- Catalog Number
- RK033 FDA UDI
- Primary DI / UDI-DI
- 10724995091122 FDA UDI
- FDA Product Code
- JOJ FDA UDI
- GMDN Term
- Chemical/physical sterilization process indicator 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
Verdoc by Albert Browne , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K140515 also covers:
K172746 also covers:
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 7450c81a-ca1f-4183-8e57-9367905d406a 38 fields · synced May 30, 2026