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Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Urine analyser IVD, laboratory, semi-automated FDA UDI
Device Name
Semi-Auto Urine Analyzer For Urine Light Weight Compact Design Full Duplex Communication Interface Internal/external Printer Interface Easy Cleaning Display in 8 Languages UAREADER2 FDA UDI
Model / Reference
UAREADER2 FDA UDI
Description
Semi-Auto Urine Analyzer For Urine Light Weight Compact Design Full Duplex Communication Interface Internal/external Printer Interface Easy Cleaning Display in 8 Languages UAREADER2 FDA UDI

Identifiers

Catalog Number
UAREADER2 FDA UDI
Primary DI / UDI-DI
10885380175596 FDA UDI
FDA Product Code
KQO FDA UDI
GMDN Term
Urine analyser IVD, laboratory, semi-automated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2900 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

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urine analyser IVD, laboratory, semi-automated

Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urine analyser IVD, laboratory, semi-automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 35a12666-031b-4dc7-a550-32f830f9c08d 35 fields · synced Jun 8, 2026