← Back to catalogue

Stryker

FDA UDI

Class II (US FDA UDI)

by Terragene S.a.

Identity

Trade Name
Stryker FDA UDI
Generic Name
Biological sterilization indicator FDA UDI
Device Name
Sterizone Rapid BI – Low Temp. Self-contained Biological Indicator for monitoring hydrogen peroxide sterilization processes FDA UDI
Model / Reference
SRBI30 FDA UDI
Description
Sterizone Rapid BI – Low Temp. Self-contained Biological Indicator for monitoring hydrogen peroxide sterilization processes FDA UDI

Identifiers

Primary DI / UDI-DI
07798164678793 FDA UDI
FDA Product Code
FRC FDA UDI
GMDN Term
Biological sterilization 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: Biological sterilization indicator

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

Similar devices

Also classified as Biological sterilization indicator.

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
Terragene S.a.

Sources (1)

  • FDA UDI 37ef361b-3ec4-48fc-95b2-4379ffffc705 34 fields · synced May 30, 2026