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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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NYLEX — 4 UDI-DI variants, MDR (Laboratoires URGO HEALTHCARE)

MD Atlas
Laboratoires URGO HEALTHCARE

Data from EUDAMED, last updated May 19, 2026

NYLEX

3664492LUHUS0043PK

4 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3664492LUHUS0043PK
Device name: NYLEX
Device model: NYLEX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 21, 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01FWDS6DN3PJ8TG06CEXS7FZCF

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

NYLEX03664492001159
NYLEX03664492001180
NYLEX03664492001166
NYLEX03664492001173