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Verdoc

FDA UDI

Class II (US FDA UDI)

by Albert Browne , Ltd.

Identity

Trade Name
VERDOC FDA UDI
Generic Name
Chemical/physical sterilization process indicator FDA UDI
Device Name
The Verdoc Steam and EO Load Data Cards indicate that a load has been processed in a steam sterilization cycle. FDA UDI
Model / Reference
RK028 FDA UDI
Description
The Verdoc Steam and EO Load Data Cards indicate that a load has been processed in a steam sterilization cycle. FDA UDI

Identifiers

Catalog Number
RK028 FDA UDI
Primary DI / UDI-DI
10724995090217 FDA UDI
FDA Product Code
JOJ FDA UDI
GMDN Term
Chemical/physical sterilization process indicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 FDA UDI
Commercial Distribution
Not 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

Verdoc by Albert Browne , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f0fc7a6c-8f20-4578-adb2-45e933dbc90b 36 fields · synced May 29, 2026