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V-Pro

FDA UDI

Class II (US FDA UDI)

by Steris Mexico, S. de R.L. de C.V.

Identity

Trade Name
V-PRO FDA UDI
Generic Name
Hydrogen peroxide gas sterilizer FDA UDI
Device Name
The V-PRO s2 Low Temperature Sterilization System is used in the terminal sterilization of properly prepared, cleaned, rinsed and dried medical devices utilizing VAPROX HC Sterilant. FDA UDI
Model / Reference
S2 FDA UDI
Description
The V-PRO s2 Low Temperature Sterilization System is used in the terminal sterilization of properly prepared, cleaned, rinsed and dried medical devices utilizing VAPROX HC Sterilant. FDA UDI

Identifiers

Catalog Number
VP60002401 FDA UDI
Primary DI / UDI-DI
00724995164096 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
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

Category: Hydrogen peroxide gas sterilizer

V-Pro by Steris Mexico, S. de R.L. de C.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hydrogen peroxide gas sterilizer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Mexico, S. de R.L. de C.V.

Sources (1)

  • FDA UDI 8e2235ea-ac39-4a7f-859b-83c7dcd08843 35 fields · synced May 31, 2026