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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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Shock absorber kit for medical crutch — 10 UDI-DI variants, MDR

MD Atlas
ELODIE SAS

Data from EUDAMED, last updated May 19, 2026

Shock absorber kit for medical crutch

37700398954D1A21320A-A0SK

10 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: ELODIE SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37700398954D1A21320A-A0SK
Device name: Shock absorber kit for medical crutch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: ELODIE SAS
SRN: FR-MF-000046262
Country: France
Email: contact@elo-d.com
Phone: 0673784968

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01K47M8F5WMZT5P5BC1Q9C45Y3

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

Elo-D03770039895089
Elo-D03770039895010
Elo-D03770039895034
Elo-D03770039895058
Elo-D03770039895041
Elo-D03770039895072
Elo-D03770039895096
Elo-D03770039895003
Elo-D03770039895027
Elo-D03770039895065