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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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Module Endoscopique Easytouch — 7 UDI-DI variants, MDR (Soluscope SAS)

MD Atlas
Soluscope SAS

Data from EUDAMED, last updated May 19, 2026

Module Endoscopique Easytouch

359761SS0161E2EQ9Y

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: Soluscope SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 359761SS0161E2EQ9Y
Device name: Module Endoscopique Easytouch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: Soluscope SAS
SRN: FR-MF-000011763
Country: France
Email: contact@anios.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KEFKQYZ9T9G27D7JJHPK5JEA

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

406700MET006503597610668166
406700MET007603597610672804
406700MET006603597610668180
406700MET006703597610669231
406700MET007003597610670411
406700MET007103597610670480
406700MET006903597610669408