TRUEtrack (UDI TRUEtrack BLOOD GLUCOSE MONITORING SYSTEM NOT FOR RETAIL SALE)
Manufactured by TRIVIDIA HEALTH, INC.
Device Regulatory Overview
The TRUEtrack (Model/Catalog Number: TRUEtrack BLOOD GLUCOSE MONITORING SYSTEM NOT FOR RETAIL SALE) 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
- TRUEtrack BLOOD GLUCOSE MONITORING SYSTEM NOT FOR RETAIL SALE
- Product Code / EMDN
- NBW
- Device Name
- TRUEtrack BLOOD GLUCOSE MONITORING SYSTEM NOT FOR RETAIL SALE
- 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 TRUEtrack?
The registered manufacturer of record for TRUEtrack is TRIVIDIA HEALTH, INC..
What is the Primary UDI-DI identifier for TRUEtrack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TRUEtrack BLOOD GLUCOSE MONITORING SYSTEM NOT FOR RETAIL SALE.
What classification code is assigned to this device?
This device is registered under product classification code NBW.
Similar Classification Devices (NBW)
Other Devices by TRIVIDIA HEALTH, INC.
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