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qUAntify

FDA UDI

Class I (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
qUAntify FDA UDI
Generic Name
Multiple urine analyte IVD, control FDA UDI
Device Name
qUAntify Control Bilevel (A liquid dipstick urine control.) FDA UDI
Model / Reference
975 FDA UDI
Description
qUAntify Control Bilevel (A liquid dipstick urine control.) FDA UDI

Identifiers

Catalog Number
975 FDA UDI
Primary DI / UDI-DI
00847661003281 FDA UDI
510(k) Number
K042446 FDA UDI
FDA Product Code
JJW FDA UDI
GMDN Term
Multiple urine analyte IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

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: Multiple urine analyte IVD, control

qUAntify by Bio-Rad Laboratories — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple urine analyte IVD, control.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3751958c-e907-4662-82f7-91e0ffa7d009 37 fields · synced May 30, 2026