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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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Stérilux ES — 9 UDI-DI variants, MDR

MD Atlas
Laboratoires PAUL HARTMANN S.à.r.l

Data from EUDAMED, last updated May 19, 2026

Stérilux ES

32614810824C

9 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 PAUL HARTMANN S.à.r.l

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 32614810824C
Device name: Stérilux ES
Device model: 1082
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 29, 2024

Manufacturer & authorised representative

Manufacturer

Name: Laboratoires PAUL HARTMANN S.à.r.l
SRN: FR-MF-000004029
Country: France
Email: sandrine.verlaine@hartmann.info

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01HWMDVKTMSP15FJR3CPNEWCE8

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

Stérilux® ES03261481000058
Stérilux® ES03261481000027
Stérilux® ES03261480000271
Stérilux® ES03261481000034
Stérilux® ES03261480000196
Stérilux® ES03261480000318
Stérilux® ES03261480000233
Stérilux® ES03261480000394
Stérilux® ES03261480000356