eudamed_udi Primary ID: 03111790259541

Venoflex Secret (UDI 03111790259541)

Manufactured by THUASNE

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Venoflex Secret (Model/Catalog Number: 59200120100313) is a medical device manufactured by THUASNE. This product is indexed under FDA Product Code / Category Classification M030405 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 59200120100313
Product Code / EMDN: M030405
Device Name: Venoflex Secret
Database Sync Date: 2026-08-09 16:28:46

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 Venoflex Secret?

The registered manufacturer of record for Venoflex Secret is THUASNE.

What is the Primary UDI-DI identifier for Venoflex Secret?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03111790259541.

What classification code is assigned to this device?

This device is registered under product classification code M030405.

Similar Classification Devices (M030405)

Other Devices by THUASNE

Programmatic Export

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

JSON API Endpoint