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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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Power Wheelchair Rehab — 13 UDI-DI variants, MDR

MD Atlas
Sunrise Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Power Wheelchair Rehab

4050063pwcrehabYN

13 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: 4050063pwcrehabYN
Device name: Power Wheelchair Rehab
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 12, 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

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GCS8D2Z3XDKP3PPBQWZEDD6M

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

Q300 M04050063058957
Q300 M Mini04050063058636
Q300 R04050063058643
Q400 F04050063058841
Q400 M04050063058858
Q400 R04050063058629
Q500 F04050063058698
Q500 H04050063058704
Q500 M04050063058711
Q500 R04050063058728
Salsa M204050063057295
Quickie Salsa R204050063056656
Zippie Salsa R204050063057301