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UASure Blood Uric Acid Test Strip

FDA UDI

Class I (US FDA UDI)

by Apex Biotechnology Corp.

Identity

Trade Name
UASure Blood Uric Acid Test Strip FDA UDI
Generic Name
Uric acid monitoring system IVD, home-use FDA UDI
Device Name
25s FDA UDI
Model / Reference
UASure I FDA UDI
Description
25s FDA UDI

Identifiers

Primary DI / UDI-DI
04713648766479 FDA UDI
FDA Product Code
LFQ FDA UDI
GMDN Term
Uric acid monitoring system IVD, home-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1775 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Uric acid monitoring system IVD, home-use

UASure Blood Uric Acid Test Strip by Apex Biotechnology Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uric acid monitoring system IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0aecdc63-fe2e-4ad0-b00b-44281be891fd 33 fields · synced May 31, 2026