GUDIDData
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eudamed_udi Primary ID: 03700659401186

Ventea S (UDI 03700659401186)

Manufactured by SEFAM

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ventea S - Primary ID 03700659401186

Device Regulatory Overview

The Ventea S (Model/Catalog Number: M-117023) 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-117023
Product Code / EMDN
Z12030103
Device Name
NÊa Duo
Database Sync Date
2026-08-09 16:48:48

Full Regulatory Attributes

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

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Frequently Asked Questions

Who is the primary manufacturer of Ventea S?

The registered manufacturer of record for Ventea S is SEFAM.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700659401186.

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

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