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

10.680/I-L/4645304255942217658
10.610-2/5443504260727752668
10.610-1/HK5/5252404255942204504
10.610-1/6045404260727752781
10.610-1/3434404255942200896
10.610-1/HKM/5140404255942201725
10.610-1/HK/4543404255942200773
10.681/I-C/4343504255942217610
10.610-1/HK/4243404260727754136
10.610-2/I/4543504260727751555
10.610-1/3843404260727752033
10.680/4442304260727753887
10.610-2/RG60/I/4343504260727751678
10.610-2/HKM/3436504255942207918
10.610-1/I/RS/5044404255942207208
10.610-2/5843504260727752743
10.610-2/4242504255942202180
10.680/3844304260727753719
10.610-1/6043404260727752767
10.610-2/5545504260727752699
10.682/3434804260727753580
10.680/I/4343304260727757878
10.610-1/BIND/3840404255942203415
10.610-2/I/4646504260727751579
10.680/I/4645304260727757892