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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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RheelaxX orthopedic insoles — 4 UDI-DI variants, MDR (YAER SARL)

MD Atlas
YAER SARL

Data from EUDAMED, last updated May 19, 2026

RheelaxX orthopedic insoles

3770029747RHEA4

4 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: YAER SARL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770029747RHEA4
Device name: RheelaxX orthopedic insoles
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: YAER SARL
SRN: FR-MF-000045665
Country: France
Email: xavier.fresnel@hotmail.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JPR86H4WPC12YTVG6BQ2CENF

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

RheelaxX03770029747008
RheelaxX03770029747022
RheelaxX03770029747039
RheelaxX03770029747015