eudamed_udi Primary ID: 03701126709378

Pied à sérum (UDI 03701126709378)

Manufactured by COMED SAS

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Pied à sérum (Model/Catalog Number: 45 410 05) is a medical device manufactured by COMED SAS. This product is indexed under FDA Product Code / Category Classification Z12030399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 45 410 05
Product Code / EMDN: Z12030399
Device Name: Pied à sérum
Database Sync Date: 2026-08-09 18:39:13

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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Frequently Asked Questions

Who is the primary manufacturer of Pied à sérum?

The registered manufacturer of record for Pied à sérum is COMED SAS.

What is the Primary UDI-DI identifier for Pied à sérum?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701126709378.

What classification code is assigned to this device?

This device is registered under product classification code Z12030399.

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