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

10.681/4342504255942205990
10.610-2/RG60/I/5644504260727751821
10.682/4040804255942201329
10.683/60501004255942216040
10.610-1/I/3843404260727751456
10.610-5/4842504255942202760
10.610-1/I/N/4343404260727751418
10.610-1/HK5/4942404260727754211
10.610-2/RG60/I/5244504260727751784
10.610-2/RG60/I/4543504260727751692
10.681/I/4450504255942201886
10.680/4742304255942205037
10.610-2/5040504260727752521
10.610-2/4246504255942202913
10.683/49431004255942200452
10.610-2/I/4244504260727751661
10.681/4340504255942205433
10.610-1/BIND/4942404260727755010
10.610-3/5843604260727758714
10.610-1/HKM/3236404255942202722
10.610/HKM/3232304255942207895
10.681/3840504260727758332
10.610-1/3842404260727752019
10.610-2/5043404260727752576
10.610-1/5143404260727752613

1 2 3 4 5