eudamed_udi Primary ID: 03701416200134

Unspecified Brand (UDI 03701416200134)

Manufactured by EUROMI

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 1214LMEW-5300) is a medical device manufactured by EUROMI. This product is indexed under FDA Product Code / Category Classification L250301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1214LMEW-5300
Product Code / EMDN: L250301
Device Name: Canules réutilisables / Reusable cannulas
Database Sync Date: 2026-08-09 16:46:52

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is EUROMI.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701416200134.

What classification code is assigned to this device?

This device is registered under product classification code L250301.

Similar Classification Devices (L250301)

Other Devices by EUROMI

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