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ClearChem Diagnostics Inc. Creatinine (Jaffe)

FDA UDI

Class II (US FDA UDI)

by Clearchem Diagnostics Inc.

Identity

Trade Name
ClearChem Diagnostics Inc. Creatinine (Jaffe) FDA UDI
Generic Name
Creatinine IVD, reagent FDA UDI
Device Name
In Vitro Diagnostics testing kit R1:3X50mL, R2:3X10mL FDA UDI
Model / Reference
CRE1120 FDA UDI
Description
In Vitro Diagnostics testing kit R1:3X50mL, R2:3X10mL FDA UDI

Identifiers

Catalog Number
CRE1120 FDA UDI
Primary DI / UDI-DI
00852169008126 FDA UDI
FDA Product Code
CGX FDA UDI
GMDN Term
Creatinine IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1225 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 — 180 Milliliter FDA UDI

Category: Creatinine IVD, reagent

ClearChem Diagnostics Inc. Creatinine (Jaffe) by Clearchem Diagnostics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Creatinine IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8805e3c4-b237-404e-8e19-c5c15fc6de29 37 fields · synced May 30, 2026