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True Metrix

FDA UDI

Class II (US FDA UDI)

by Trividia Health, Inc.

Identity

Trade Name
TRUE METRIX FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
CVS Health TRUE METRIX Self Monitoring Blood Glucose Meter Kit FDA UDI
Model / Reference
TRUE METRIX Self Monitoring Blood Glucose Meter FDA UDI
Description
CVS Health TRUE METRIX Self Monitoring Blood Glucose Meter Kit FDA UDI

Identifiers

Catalog Number
RE4007-01 FDA UDI
Primary DI / UDI-DI
00050428275283 FDA UDI
FDA Product Code
LFR FDA UDI
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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose monitoring system IVD, home-use

True Metrix by Trividia Health, 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

Sources (1)

  • FDA UDI f67ba236-85c8-4b35-b2f1-f2a838d26105 36 fields · synced Jun 8, 2026