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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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Dispositif médical destiné au recueil… — 2 UDI-DI variants, MDR

MD Atlas
CLEANIS

Data from EUDAMED, last updated May 19, 2026

Dispositif médical destiné au recueil des excreta

376005923RECUEILEXCDT03B4

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: CLEANIS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376005923RECUEILEXCDT03B4
Device name: Dispositif médical destiné au recueil des excreta
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: CLEANIS
SRN: FR-MF-000004677
Country: France
Email: contact-eudamed@innothera.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K3NJQ9ZF0BY6B19HD9W1CVWD

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

Gelmax® Tampon Super-absorbant 700ml boîte de 2503760059232070
Gelmax® Tampon, x 2503760059230212