Identity
- Trade Name
- AMSCO V-PRO FDA UDI
- Generic Name
- Hydrogen peroxide gas sterilizer FDA UDI
- Device Name
- The Amsco V-PRO maX Low Temperature Sterilization System is intended for use in the terminal sterilization of properly prepared (cleaned, rinsed and dried) metal and nonmetal medical devices used in Healthcare Facilities. FDA UDI
- Model / Reference
- maX FDA UDI
- Description
- The Amsco V-PRO maX Low Temperature Sterilization System is intended for use in the terminal sterilization of properly prepared (cleaned, rinsed and dried) metal and nonmetal medical devices used in Healthcare Facilities. FDA UDI
Identifiers
- Catalog Number
- VP3 FDA UDI
- Primary DI / UDI-DI
- 00724995151997 FDA UDI
- FDA Product Code
- MLR FDA UDI
- GMDN Term
- Hydrogen peroxide gas sterilizer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6860 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Amsco V-Pro by Steris Mexico, S. de R.L. de C.V. — 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
- Steris Mexico, S. de R.L. de C.V.
Sources (1)
- FDA UDI d6013069-ed02-46f0-9a76-7c6e87dd072c 36 fields · synced May 30, 2026