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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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LUCEA LED — 6 UDI-DI variants, MDR (Maquet SAS)

MD Atlas
Maquet SAS

Data from EUDAMED, last updated May 19, 2026

LUCEA LED

3700712421250QX

6 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: Maquet SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3700712421250QX
Device name: LUCEA LED
Device model: Lucea 10-40
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: Maquet SAS
SRN: FR-MF-000002926
Country: France
Email: sylviane.boironbourgeois@getinge.com
Phone: +33 6 08 73 60 40

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01G9YCK8RF16PJRKPHVVDRFZ0W

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

ARDLCA309008A03700712415921
ARDLCA409005A03700712415853
ARDLCA109006A03700712415846
ARDLCA209021A03700712415877
ARDLCA309009A03700712415938
ARDLCA109001A03700712415860