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GlutarTest 1

FDA UDI

Class II (US FDA UDI)

by IBT Scientific

Identity

Trade Name
GlutarTest 1 FDA UDI
Generic Name
Glutaraldehyde device disinfectant/sterilant test strip FDA UDI
Device Name
1 bottle of 100 test strips to test glutaraldehyde FDA UDI
Model / Reference
GT23101 FDA UDI
Description
1 bottle of 100 test strips to test glutaraldehyde FDA UDI

Identifiers

Primary DI / UDI-DI
G212GT23101 FDA UDI
510(k) Number
K002011 FDA UDI
FDA Product Code
LIF FDA UDI
GMDN Term
Glutaraldehyde device disinfectant/sterilant test strip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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: Glutaraldehyde device disinfectant/sterilant test strip

GlutarTest 1 by IBT Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glutaraldehyde device disinfectant/sterilant test strip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
IBT Scientific

Sources (1)

  • FDA UDI 2d0062fb-008d-41cd-9e74-76e40f00a764 35 fields · synced Jun 8, 2026