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Biotrace™

FDA UDI

Class II (US FDA UDI)

by Terragene S.a.

Identity

Trade Name
BIOTRACE™ FDA UDI
Generic Name
Biological sterilization indicator reader FDA UDI
Device Name
BIOTRACE™ Rapid Read 5 VH2O2 Biological Indicator Reader FDA UDI
Model / Reference
73420 FDA UDI
Description
BIOTRACE™ Rapid Read 5 VH2O2 Biological Indicator Reader FDA UDI

Identifiers

Primary DI / UDI-DI
07798375772495 FDA UDI
510(k) Number
K221641 FDA UDI
FDA Product Code
FRC FDA UDI
GMDN Term
Biological sterilization indicator reader 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

Yes

FDA UDI

Category: Biological sterilization indicator reader

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

Similar devices

Also classified as Biological sterilization indicator reader.

Cleared under the same submission

K221641 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 d6c8e1ea-bc3d-4e58-b6b2-0be1c4ab9f4e 36 fields · synced Jun 8, 2026