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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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E-Mobility device — 5 UDI-DI variants, MDR (Sunrise Medical GmbH)

MD Atlas
Sunrise Medical GmbH

Data from EUDAMED, last updated May 23, 2026

E-Mobility device

4050063emobilityMJ

5 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: Sunrise Medical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4050063emobilityMJ
Device name: E-Mobility device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 29, 2022

Manufacturer & authorised representative

Manufacturer

Name: Sunrise Medical GmbH
SRN: DE-MF-000006320
Country: Germany
Email: kundenservice@sunrisemedical.de
Phone: +4972539800

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G94V70SE6GX3MZREVDR8RWC7

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

Attitude04050063056915
F3504050063059381
F5504050063058780
R2004050063059367
StreetJet04050063060332