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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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URGO ULTRA PROTECTEUR — 2 UDI-DI variants, MDR

MD Atlas
Laboratoires URGO HEALTHCARE

Data from EUDAMED, last updated May 19, 2026

URGO ULTRA PROTECTEUR

3664492LUHUS0010P4

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Laboratoires URGO HEALTHCARE

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Device characteristics

Animal tissues / cells

Identity & classification

Basic UDI-DI: 3664492LUHUS0010P4
Device name: URGO ULTRA PROTECTEUR
Device model: URGO ULTRA PROTECTEUR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: Laboratoires URGO HEALTHCARE
SRN: FR-MF-000001538
Country: France
Email: info@laboratoiresurgo.fr

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FXJAAEQVXNVERQ4K07MYW2PT

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

URGO ULTRA-PROTECTEUR03664492000756
URGO ULTRA-PROTECTION03664492019741