TRUE METRIX PRO (UDI TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER)
Manufactured by TRIVIDIA HEALTH, INC.
Device Regulatory Overview
The TRUE METRIX PRO (Model/Catalog Number: TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER) 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 PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER
- Product Code / EMDN
- LFR
- Device Name
- PROCURE TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE METER
- Database Sync Date
- 2026-08-09 09:00:33
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)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.
What classification code is assigned to this device?
This device is registered under product classification code LFR.
Similar Classification Devices (LFR)
Other Devices by TRIVIDIA HEALTH, INC.
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