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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
TRUE METRIX PRE-PACK - USE ONLY FOR MEDICARE AND MEDICAID FDA UDI
Model / Reference
TRUE METRIX PRE-PACK - USE ONLY FOR MEDICARE AND MEDICAID FDA UDI
Description
TRUE METRIX PRE-PACK - USE ONLY FOR MEDICARE AND MEDICAID FDA UDI

Identifiers

Catalog Number
RE4H01-75 FDA UDI
Primary DI / UDI-DI
10021292007000 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
Not 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

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

True Metrix by Trividia Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0b1cf1fe-3418-45ab-808b-dee0cc5d583c 37 fields · synced Jun 8, 2026