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Urine Chemistry Control Bi-Level

FDA UDI

Class I (US FDA UDI)

by Cliniqa Corporation

Identity

Trade Name
Urine Chemistry Control Bi-Level FDA UDI
Generic Name
Multiple urine analyte IVD, control FDA UDI
Device Name
Urine Chemistry Control Bi-Level FDA UDI
Model / Reference
97105 FDA UDI
Description
Urine Chemistry Control Bi-Level FDA UDI

Identifiers

Primary DI / UDI-DI
00817238010318 FDA UDI
510(k) Number
K082107 FDA UDI
FDA Product Code
JJY 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

No

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

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

Urine Chemistry Control Bi-Level by Cliniqa Corporation — 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

K082107 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cliniqa Corporation

Sources (1)

  • FDA UDI 1ea84233-0ad4-4971-98f9-13df56b43726 34 fields · synced Jun 1, 2026