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ClearChem Diagnostics Inc. Bilirubin, Direct

FDA UDI

Class II (US FDA UDI)

by Clearchem Diagnostics Inc.

Identity

Trade Name
ClearChem Diagnostics Inc. Bilirubin, Direct FDA UDI
Generic Name
Conjugated (direct) bilirubin IVD, reagent FDA UDI
Device Name
In Vitro Diagnostics testing kit R1:3X28mL, R2:3X7mL FDA UDI
Model / Reference
BRD1050 FDA UDI
Description
In Vitro Diagnostics testing kit R1:3X28mL, R2:3X7mL FDA UDI

Identifiers

Catalog Number
BRD1050 FDA UDI
Primary DI / UDI-DI
00852169008096 FDA UDI
FDA Product Code
CIG FDA UDI
GMDN Term
Conjugated (direct) bilirubin IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1110 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 — 105 Milliliter FDA UDI

Category: Conjugated (direct) bilirubin IVD, reagent

ClearChem Diagnostics Inc. Bilirubin, Direct by Clearchem Diagnostics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Conjugated (direct) bilirubin IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fbc9246e-a1c0-4c26-a7aa-38b07a5f1fb1 37 fields · synced May 30, 2026