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Vaprox

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
VAPROX FDA UDI
Generic Name
Hydrogen peroxide device sterilant FDA UDI
Device Name
VAPROX HC Sterilant is 59 percent Hydrogen Peroxide used with V-PRO Low Temperature Sterilization Systems. The cup carries RFID tag. Net contents 4-29.6 mL per cup. FDA UDI
Model / Reference
PB012 FDA UDI
Description
VAPROX HC Sterilant is 59 percent Hydrogen Peroxide used with V-PRO Low Temperature Sterilization Systems. The cup carries RFID tag. Net contents 4-29.6 mL per cup. FDA UDI

Identifiers

Catalog Number
PB012 FDA UDI
Primary DI / UDI-DI
00724995153106 FDA UDI
510(k) Number
K172754 FDA UDI
K182568 FDA UDI
K190103 FDA UDI
K190917 FDA UDI
K222093 FDA UDI
K233065 FDA UDI
FDA Product Code
MLR FDA UDI
GMDN Term
Hydrogen peroxide device sterilant 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

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

No

FDA UDI

Category: Hydrogen peroxide device sterilant

Vaprox by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hydrogen peroxide device sterilant.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 050e050a-5edb-43e6-b9a2-bcec3f623f68 36 fields · synced Jun 8, 2026