GUDIDData
gudid Primary ID: TRUE METRIX SELF MONITORING BLOOD GLUCOSE TEST STRIPS - 25 Test Strips

TRUE METRIX (UDI TRUE METRIX SELF MONITORING BLOOD GLUCOSE TEST STRIPS - 25 Test Strips)

Manufactured by TRIVIDIA HEALTH, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRUE METRIX - Primary ID TRUE METRIX SELF MONITORING BLOOD GLUCOSE TEST STRIPS - 25 Test Strips

Device Regulatory Overview

The TRUE METRIX (Model/Catalog Number: TRUE METRIX SELF MONITORING BLOOD GLUCOSE TEST STRIPS - 25 Test Strips) is a medical device manufactured by TRIVIDIA HEALTH, INC.. This product is indexed under FDA Product Code / Category Classification LFR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TRUE METRIX SELF MONITORING BLOOD GLUCOSE TEST STRIPS - 25 Test Strips
Product Code / EMDN
LFR
Device Name
TRUE METRIX SELF MONITORING BLOOD GLUCOSE TEST STRIPS - 25 Test Strips
Database Sync Date
2026-08-09 09:00:33

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of TRUE METRIX?

The registered manufacturer of record for TRUE METRIX is TRIVIDIA HEALTH, INC..

What is the Primary UDI-DI identifier for TRUE METRIX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TRUE METRIX SELF MONITORING BLOOD GLUCOSE TEST STRIPS - 25 Test Strips.

What classification code is assigned to this device?

This device is registered under product classification code LFR.

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