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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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MOBILITÉ COUCHÉE PASSIVE — 7 UDI-DI variants, MDR

MD Atlas
ALTER ÉCO SANTÉ SAS

Data from EUDAMED, last updated May 19, 2026

MOBILITÉ COUCHÉE PASSIVE

376031137MOBICOPARF

7 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: ALTER ÉCO SANTÉ SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376031137MOBICOPARF
Device name: MOBILITÉ COUCHÉE PASSIVE
Device model: MOBILITÉ COUCHÉE PASSIVE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 23, 2024

Manufacturer & authorised representative

Manufacturer

Name: ALTER ÉCO SANTÉ SAS
SRN: FR-MF-000003051
Country: France
Email: contact@alterecosante.net
Phone: +33 5 344 60 376

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01J5ZNK1TD14MGF24WDVY0MR90

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

ALESOLI MAD13003760311370052
ALESOLI MAD20003760311371110
PROGLISS PRO11003760311372360
PROGLISS PRO13003760311372162
PROGLISS PRO14003760311372377
PROGLISS PRO20003760311372155
SANGLE POULIE03760311370915