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Glucose Reagent

FDA UDI

Class II (US FDA UDI)

by DIAMOND DIAGNOSTICS Inc

Identity

Trade Name
Glucose Reagent FDA UDI
Generic Name
Glucose IVD, kit, electrometry FDA UDI
Device Name
For the quantitative determination of glucose in serum, plasma, urine and cerebrospinal fluid. FDA UDI
Model / Reference
BK-443355D FDA UDI
Description
For the quantitative determination of glucose in serum, plasma, urine and cerebrospinal fluid. FDA UDI

Identifiers

Primary DI / UDI-DI
00811403011131 FDA UDI
FDA Product Code
CGA FDA UDI
GMDN Term
Glucose IVD, kit, electrometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose IVD, kit, electrometry

Glucose Reagent by DIAMOND DIAGNOSTICS Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose IVD, kit, electrometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 15a3dd87-a969-402f-96bd-12865e30476f 33 fields · synced May 30, 2026