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AgaMatrix

FDA UDI

Class II (US FDA UDI)

by Agamatrix, Inc.

Identity

Trade Name
AgaMatrix FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
Test Strips, AgaMatrix, Jazz, 10CT FDA UDI
Model / Reference
8000-10474 FDA UDI
Description
Test Strips, AgaMatrix, Jazz, 10CT FDA UDI

Identifiers

Primary DI / UDI-DI
00385541001908 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Glucose monitoring system IVD, home-use 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

No

FDA UDI

Over-the-Counter

Yes

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 monitoring system IVD, home-use

AgaMatrix by Agamatrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose monitoring system IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Agamatrix, Inc.

Sources (1)

  • FDA UDI 52031f67-b45b-47a6-aa46-c11f53ed8dae 35 fields · synced May 30, 2026