eudamed_udi Primary ID: 03701126703215

Spéculums auriculaires à usage unique (UDI 03701126703215)

Manufactured by COMED SAS

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Spéculums auriculaires à usage unique (Model/Catalog Number: 24 700 40B) is a medical device manufactured by COMED SAS. This product is indexed under FDA Product Code / Category Classification Z12149085 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 24 700 40B
Product Code / EMDN: Z12149085
Device Name: Spéculum auriculaire à usage unique
Database Sync Date: 2026-08-09 17:26:08

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 Spéculums auriculaires à usage unique?

The registered manufacturer of record for Spéculums auriculaires à usage unique is COMED SAS.

What is the Primary UDI-DI identifier for Spéculums auriculaires à usage unique?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701126703215.

What classification code is assigned to this device?

This device is registered under product classification code Z12149085.

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