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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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TRANSFERT ACTIF ASSIS DEBOUT — 3 UDI-DI variants, MDR

MD Atlas
ALTER ÉCO SANTÉ SAS

Data from EUDAMED, last updated May 19, 2026

TRANSFERT ACTIF ASSIS DEBOUT

376031137TRACASDEBA7

3 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: 376031137TRACASDEBA7
Device name: TRANSFERT ACTIF ASSIS DEBOUT
Device model: TRANSFERT ACTIF ASSIS DEBOUT
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

3 UDI-DI variants

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Applied filters

basicUdiUlid01J5ZAPP2C9665EFMA2XNR6V2F

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

CEINTURE EMMA03760311370045
Diskeko03760311371028
MOUSTACHE03760311370953