Identity
- Trade Name
- VAPROX FDA UDI
- Generic Name
- Hydrogen peroxide device sterilant FDA UDI
- Device Name
- VAPROX HC Sterilant is 59 percent Hydrogen Peroxide, designed specifically for use in the V-PRO Low Temperature Sterilization Systems. The cup carries RFID tag. Net contents 3 -113 mL per cup. FDA UDI
- Model / Reference
- PB011 FDA UDI
- Description
- VAPROX HC Sterilant is 59 percent Hydrogen Peroxide, designed specifically for use in the V-PRO Low Temperature Sterilization Systems. The cup carries RFID tag. Net contents 3 -113 mL per cup. FDA UDI
Identifiers
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6860 FDA UDI
- Commercial Distribution
- 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
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
Yes
FDA UDI
Category: Hydrogen peroxide device sterilant
Vaprox by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- SPOROX® — Sultan Healthcare Inc · Class II
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Cleared under the same submission
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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
- Steris Corporation
Sources (1)
- FDA UDI b8010cdf-1327-4a5e-83c2-451b30d24a2e 36 fields · synced Jun 8, 2026