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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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Bassin de lit — 2 UDI-DI variants, MDR (GILAC)

MD Atlas
GILAC

Data from EUDAMED, last updated May 19, 2026

Bassin de lit

310041BassinEM

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: GILAC

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 310041BassinEM
Device name: Bassin de lit
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: GILAC
SRN: FR-MF-000029695
Country: France
Email: martin.bouthiaux@gilac.com
Phone: +33648731494

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GSDDJ0DK7YCMSK6VQ09D222E

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

Bassin de lit 2.5L blanc03100411011217
Bassin de lit 2.5L Cooper03100411013273