MicroStrip Urinalysis Control Bi-Level

FDA UDI

Class I (US FDA UDI)

by Cliniqa Corporation

Identity

Trade Name: MicroStrip Urinalysis Control Bi-Level FDA UDI
Generic Name: Multiple urine analyte IVD, control FDA UDI
Device Name: MicroStrip Urinalysis Control Bi-Level FDA UDI
Model / Reference: 97203 FDA UDI
Description: MicroStrip Urinalysis Control Bi-Level FDA UDI

Identifiers

Primary DI / UDI-DI: 00817238010509 FDA UDI
510(k) Number: K081908 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Multiple urine analyte IVD, control

MicroStrip Urinalysis 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.

URINALYSIS CONTROL - LEVEL 2 (URNAL CONTROL 2) — Randox Laboratories, Ltd. · Class I
Mission Liquid Urine Controls — ACON Laboratories, Inc. · Class I
iChem® VELOCITY™ — BECKMAN COULTER IRELAND INC. · Class I
ABX PENTRA URINE CONTROL L/H — Horiba Abx · Class I
K-ASSAY® Microalbumin Urine Control — KAMIYA BIOMEDICAL COMPANY, LLC · Class I
CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
Dropper Plus Point-of-Care Urinalysis Dipstick Control Level 1&2 Set 2x5mL — QUANTIMETRIX CORP. · Class I
qUAntify — Bio-Rad Laboratories · Class I

Cleared under the same submission

K081908 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Cliniqa Corporation

Sources (1)

FDA UDI 6fcb6ca4-c894-4bf5-a804-518940798d17 34 fields · synced May 30, 2026