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Verisure™

FDA UDI

Class II (US FDA UDI)

by Terragene S.a.

Identity

Trade Name
VERISURE™ FDA UDI
Generic Name
Chemical/physical sterilization process indicator FDA UDI
Device Name
VERISURE™ Bowie-Dick Test Card Kit FDA UDI
Model / Reference
73190 FDA UDI
Description
VERISURE™ Bowie-Dick Test Card Kit FDA UDI

Identifiers

Primary DI / UDI-DI
07798375772730 FDA UDI
510(k) Number
K200272 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

Yes

FDA UDI

Category: Chemical/physical sterilization process indicator

Verisure™ by Terragene S.a. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chemical/physical sterilization process indicator.

Cleared under the same submission

K200272 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terragene S.a.

Sources (1)

  • FDA UDI 84f83d8e-ad7e-4d0b-bcea-c7962d097324 36 fields · synced May 30, 2026