eudamed_udi Primary ID: 05908226260657

AFTINEX (UDI 05908226260657)

Manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AFTINEX (Model/Catalog Number: AFTINEX Ulcer Gel packaged in a 10ml tube in a carton with instructions for use. Language version: Polish) is a medical device manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification M9002 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AFTINEX Ulcer Gel packaged in a 10ml tube in a carton with instructions for use. Language version: Polish
Product Code / EMDN: M9002
Device Name: Ulcer Gel / Żel na afty
Database Sync Date: 2026-08-09 16:30:04

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 AFTINEX?

The registered manufacturer of record for AFTINEX is LABORATOIRE L'IDEAL Parisien Sp. z o.o..

What is the Primary UDI-DI identifier for AFTINEX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05908226260657.

What classification code is assigned to this device?

This device is registered under product classification code M9002.

Similar Classification Devices (M9002)

Other Devices by LABORATOIRE L'IDEAL Parisien Sp. z o.o.

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