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Test Kits

FDA UDI

Class I (US FDA UDI)

by Microbiologics, Inc.

Identity

Trade Name
Test Kits FDA UDI
Generic Name
Multiple non-Enterobacteriaceae species culture isolate identification IVD, reagent FDA UDI
Device Name
Oxidase Swabs FDA UDI
Model / Reference
60500 FDA UDI
Description
Oxidase Swabs FDA UDI

Identifiers

Catalog Number
60500 FDA UDI
Primary DI / UDI-DI
10634853001357 FDA UDI
FDA Product Code
JTO FDA UDI
GMDN Term
Multiple non-Enterobacteriaceae species culture isolate identification IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple non-Enterobacteriaceae species culture isolate identification IVD, reagent

Test Kits by Microbiologics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6982635a-c0a5-44bd-98d9-09ef26b671ec 36 fields · synced Jun 1, 2026