eudamed_udi
Primary ID: 15065023763983
TruReno (UDI 15065023763983)
Manufactured by BioFynder Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TruReno - Primary ID 15065023763983
Device Regulatory Overview
The TruReno (Model/Catalog Number: TR10002) is a medical device manufactured by BioFynder Limited. This product is indexed under FDA Product Code / Category Classification W0101060101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TR10002
- Product Code / EMDN
- W0101060101
- Device Name
- Blood Glucose Test Strips
- Database Sync Date
- 2026-08-09 16:30:12
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 TruReno?
The registered manufacturer of record for TruReno is BioFynder Limited.
What is the Primary UDI-DI identifier for TruReno?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15065023763983.
What classification code is assigned to this device?
This device is registered under product classification code W0101060101.
Similar Classification Devices (W0101060101)
Other Devices by BioFynder Limited
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