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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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Eden e — 7 UDI-DI variants, MDR (Innov'SA)

MD Atlas
Innov'SA

Data from EUDAMED, last updated May 19, 2026

Eden e

3665533EDENEUK

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: Innov'SA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3665533EDENEUK
Device name: Eden e
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Innov'SA
SRN: FR-MF-000006814
Country: France
Email: boite.innovsa@innovsa.com
Phone: +33 325294000

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ9Q6KWX362G4G51173HP3FW

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

Eden e - Bleu Lagon03665533123274
Eden e - Gris Chiné03665533055865
Eden e - Gris Galet03665533064805
Eden e - Velours Galène03665533055896
Eden e - Velours Marron03665533064812
Eden e - Velours Saphir03665533055889
Eden e 600 - Velours Galène03665533124141