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Microorganism Pellets

FDA UDI

Class I (US FDA UDI)

by Microbiologics, Inc.

Identity

Trade Name
Microorganism Pellets FDA UDI
Generic Name
Multiple urine analyte IVD, control FDA UDI
Device Name
Culture Control Kit for Uricult FDA UDI
Model / Reference
URI-KIT FDA UDI
Description
Culture Control Kit for Uricult FDA UDI

Identifiers

Catalog Number
URI-KIT FDA UDI
Primary DI / UDI-DI
10634853000589 FDA UDI
FDA Product Code
JTR FDA UDI
GMDN Term
Multiple urine analyte IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2480 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

Yes

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 urine analyte IVD, control

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

Similar devices

Also classified as Multiple urine analyte IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f7f450e3-2f46-4028-b924-b95dbaf8541a 36 fields · synced May 31, 2026