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Verify

FDA UDI

Class II (US FDA UDI)

by Albert Browne , Ltd.

Identity

Trade Name
VERIFY FDA UDI
Generic Name
Chemical/physical sterilization process indicator FDA UDI
Device Name
The VERIFY SixCess 250F 30 Minute Indicator Long are cycle verification indicators which are designed to react to all critical variables for specific sterilization cycles. FDA UDI
Model / Reference
PCC007 FDA UDI
Description
The VERIFY SixCess 250F 30 Minute Indicator Long are cycle verification indicators which are designed to react to all critical variables for specific sterilization cycles. FDA UDI

Identifiers

Catalog Number
PCC007 FDA UDI
Primary DI / UDI-DI
10724995084636 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
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: Chemical/physical sterilization process indicator

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

Similar devices

Also classified as Chemical/physical sterilization process indicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Albert Browne , Ltd.

Sources (1)

  • FDA UDI 93f5770b-980e-4a41-89de-8b99d2f2042d 35 fields · synced Jun 1, 2026