GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 03700659401193

Ventea ST (UDI 03700659401193)

Manufactured by SEFAM

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ventea ST - Primary ID 03700659401193

Device Regulatory Overview

The Ventea ST (Model/Catalog Number: M-117024) is a medical device manufactured by SEFAM. This product is indexed under FDA Product Code / Category Classification Z12030103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
M-117024
Product Code / EMDN
Z12030103
Device Name
NÊa Duo
Database Sync Date
2026-08-09 18:11:57

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 Ventea ST?

The registered manufacturer of record for Ventea ST is SEFAM.

What is the Primary UDI-DI identifier for Ventea ST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700659401193.

What classification code is assigned to this device?

This device is registered under product classification code Z12030103.

Similar Classification Devices (Z12030103)

Other Devices by SEFAM

Programmatic Export

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

JSON API Endpoint