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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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Walking — 11 UDI-DI variants, MDR (R82 A/S)

MD Atlas
R82 A/S

Data from EUDAMED, last updated May 23, 2026

Walking

570729212060627

11 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: R82 A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 570729212060627
Device name: —
Device model: Walking
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: R82 A/S
SRN: DK-MF-000000772
Country: Denmark
Email: R82@etac.com

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01KJZ8HWFBA029JJW4HAZZJSQN

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

Crocodile05707292355942
Crocodile05707292355959
Crocodile05707292930392
Crocodile05715393021949
Crocodile05715393021956
Crocodile05707292547026
Crocodile05715393021963
Mustang05707292553102
Mustang05707292604019
Mustang05707292604064
Mustang05707292604088