← Back to catalogue

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: The VAPROX HC Sterilant uses 59 percent Hydrogen Peroxide and is used with V-PRO Low Temperature Sterilization Systems. The net contents are 113 mL per cup. FDA UDI
Model / Reference: PB007 FDA UDI
Description: The VAPROX HC Sterilant uses 59 percent Hydrogen Peroxide and is used with V-PRO Low Temperature Sterilization Systems. The net contents are 113 mL per cup. FDA UDI

Identifiers

Catalog Number: PB007 FDA UDI
Primary DI / UDI-DI: 00724995089160 FDA UDI
510(k) Number: K062297 FDA UDI
K083097 FDA UDI
K102330 FDA UDI
K102394 FDA UDI
K111810 FDA UDI
K112760 FDA UDI
K112813 FDA UDI
K120632 FDA UDI
K131120 FDA UDI
K140498 FDA UDI
K160433 FDA UDI
K162413 FDA UDI
K172319 FDA UDI
K172754 FDA UDI
K182568 FDA UDI
K190103 FDA UDI
K190917 FDA UDI
K222093 FDA UDI
K223476 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

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

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.

Liquid Ultra — CROSSTEX INTERNATIONAL, INC. · Class I
Sterling Medical Products — APOLLO MEDICAL PRODUCTS CORP.
Sterrad — ADVANCED STERILIZATION PRODUCTS SERVICES INC. · Class II
125-280 Solution™ for STERIZONE VP4 Sterilizer — Tso3, Inc. · Class II
Sterrad — ADVANCED STERILIZATION PRODUCTS SERVICES INC. · Class II
SPOROX® II — Sultan Healthcare Inc · Class II
SPOROX® — Sultan Healthcare Inc · Class II
Sterrad — ADVANCED STERILIZATION PRODUCTS SERVICES INC. · Class II

Cleared under the same submission

K172754 also covers:

VAPROX — STERIS CORPORATION
VAPROX — STERIS CORPORATION

K182568 also covers:

VAPROX — STERIS CORPORATION
VAPROX — STERIS CORPORATION

K190103 also covers:

VAPROX — STERIS CORPORATION
VAPROX — STERIS CORPORATION

K190917 also covers:

VAPROX — STERIS CORPORATION
VAPROX — STERIS CORPORATION

K222093 also covers:

VAPROX — STERIS CORPORATION
VAPROX — STERIS CORPORATION

K233065 also covers:

VAPROX — STERIS CORPORATION
VAPROX — STERIS CORPORATION

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI 86779cd0-34ab-47a8-91f5-805cb774503b 37 fields · synced Jun 8, 2026