← Back to catalogue

Urine Uric Acid Standard Kit

FDA UDI

Class II (US FDA UDI)

by Verichem Laboratories, Inc.

Identity

Trade Name
Urine Uric Acid Standard Kit FDA UDI
Generic Name
Multiple clinical chemistry protein IVD, calibrator FDA UDI
Device Name
calibrator / calibration verifier FDA UDI
Model / Reference
9020 FDA UDI
Description
calibrator / calibration verifier FDA UDI

Identifiers

Primary DI / UDI-DI
00852553007032 FDA UDI
510(k) Number
K112834 FDA UDI
FDA Product Code
JIX FDA UDI
GMDN Term
Multiple clinical chemistry protein IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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

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

Dimensions & Sizes

Size
Total Volume — 25 Milliliter FDA UDI

Category: Multiple clinical chemistry protein IVD, calibrator

Urine Uric Acid Standard Kit by Verichem Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple clinical chemistry protein IVD, calibrator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3fbe5374-abb8-4674-ba89-5af48a23ec59 37 fields · synced May 30, 2026