eudamed_udi
Primary ID: 15065026245301
TruVue (UDI 15065026245301)
Manufactured by BioFynder Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TruVue - Primary ID 15065026245301
Device Regulatory Overview
The TruVue (Model/Catalog Number: TV20043) is a medical device manufactured by BioFynder Limited. This product is indexed under FDA Product Code / Category Classification W0102050110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TV20043
- Product Code / EMDN
- W0102050110
- Device Name
- Testo Test (FIA)
- Database Sync Date
- 2026-08-09 16:46:02
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 TruVue?
The registered manufacturer of record for TruVue is BioFynder Limited.
What is the Primary UDI-DI identifier for TruVue?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15065026245301.
What classification code is assigned to this device?
This device is registered under product classification code W0102050110.
Similar Classification Devices (W0102050110)
Other Devices by BioFynder Limited
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