Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Rollstuhlkissen — 593 UDI-DI variants, MDR (Moritz Reha-Hilfen GmbH)

MD Atlas
Moritz Reha-Hilfen GmbH

Data from EUDAMED, last updated May 23, 2026

Rollstuhlkissen

426072775002A2

593 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: Moritz Reha-Hilfen GmbH

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426072775002A2
Device name: Rollstuhlkissen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Moritz Reha-Hilfen GmbH
SRN: DE-MF-000005119
Country: Germany
Email: info@rehamoritz.de
Phone: +49 (0) 5655 758 98 40

Variants by status

UDI-DI variants

593 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KM7VK4TXRXYGKHK0RVX61XD3

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

10.610-1/5349404255942204474
10.610-2/5444504255942203712
10.610-1/5342404255942204054
10.610-2/I/4043504260727751487
10.610-2/4343504260727752255
10.610-2/I/4540504260727751548
10.610-2/4756504255942201435
10.610-1/HK5/5242404260727754235
10.683/38421004260727753672
10.610-1/3648404260727751968
10.610-2/RG60/I/5545504260727751814
10.682/3634804255942201404
10.683/48431004255942207536
10.610-1/4543404260727752323
10.610-1/5243404260727752637
10.680/I/4043304260727757861
10.610-8/40401004260727755225
10.620-3/4343604260727756420
10.680/4246304260727753832
10.610-2/46425504255942201756
10.682/3642804255942203040
10.680/3337304260727753566
10.680/3840304260727753665
10.610-2/I/4040504260727751463
10.610-2/HK5/4642504260727754181

4 5 6 7 8