gudid
Primary ID: TRUE FOCUS Control Solution Level 3
TRUE FOCUS (UDI TRUE FOCUS Control Solution Level 3)
Manufactured by TRIVIDIA HEALTH, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRUE FOCUS - Primary ID TRUE FOCUS Control Solution Level 3
Device Regulatory Overview
The TRUE FOCUS (Model/Catalog Number: TRUE FOCUS Control Solution Level 3) is a medical device manufactured by TRIVIDIA HEALTH, INC.. This product is indexed under FDA Product Code / Category Classification JJX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TRUE FOCUS Control Solution Level 3
- Product Code / EMDN
- JJX
- Device Name
- TRUE FOCUS Control Solution Level 3
- 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 FOCUS?
The registered manufacturer of record for TRUE FOCUS is TRIVIDIA HEALTH, INC..
What is the Primary UDI-DI identifier for TRUE FOCUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TRUE FOCUS Control Solution Level 3.
What classification code is assigned to this device?
This device is registered under product classification code JJX.
Similar Classification Devices (JJX)
Other Devices by TRIVIDIA HEALTH, INC.
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