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V-Pro

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V-PRO FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
The 10 inch x 10 inch x 3.5 inch Sterilization Tray with Lid is used with the Sterilization Container System. FDA UDI
Model / Reference
VP0040 FDA UDI
Description
The 10 inch x 10 inch x 3.5 inch Sterilization Tray with Lid is used with the Sterilization Container System. FDA UDI

Identifiers

Catalog Number
VP0040 FDA UDI
Primary DI / UDI-DI
10724995001732 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Depth — 4 Inch FDA UDI
Width — 10 Inch FDA UDI
Length — 10 Inch FDA UDI

Category: Device sterilization/disinfection container, reusable

V-Pro by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI b36b39ac-ee9c-4a04-9724-7e2a31425487 36 fields · synced Jun 6, 2026