GUDIDData
eudamed_udi Primary ID: 15065026245004

TruReno (UDI 15065026245004)

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 15065026245004

Device Regulatory Overview

The TruReno (Model/Catalog Number: TR10005) is a medical device manufactured by BioFynder Limited. This product is indexed under FDA Product Code / Category Classification W010106010801 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TR10005
Product Code / EMDN
W010106010801
Device Name
Electrochemical control
Database Sync Date
2026-08-09 17:23:24

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

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 15065026245004.

What classification code is assigned to this device?

This device is registered under product classification code W010106010801.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint