GUDIDData
gudid Primary ID: TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER FOR MULTIPLE PATIENT

TRUE METRIX PRO (UDI TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER FOR MULTIPLE PATIENT)

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 PRO - Primary ID TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER FOR MULTIPLE PATIENT

Device Regulatory Overview

The TRUE METRIX PRO (Model/Catalog Number: TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER FOR MULTIPLE PATIENT) is a medical device manufactured by TRIVIDIA HEALTH, INC.. This product is indexed under FDA Product Code / Category Classification NBW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER FOR MULTIPLE PATIENT
Product Code / EMDN
NBW
Device Name
TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER FOR MULTIPLE PATIENT USE
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 PRO?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER FOR MULTIPLE PATIENT.

What classification code is assigned to this device?

This device is registered under product classification code NBW.

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