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

10.681/4246504255942202623
10.610-3/4040604260727752088
10.683/50431004255942201848
10.610-1/5642404255942208045
10.680/I/4843304260727757908
10.680/4042304260727753740
10.610-2/4443504260727752286
10.682/4446804255942207086
10.610-2/4541504260727758646
10.610-1/BIND/4040404260727754945
10.610-2/RG60/I/5243504260727751777
10.610-2/4143504260727752163
10.610-2/4840504260727752408
10.610-2/I-L/4343504255942200810
10.610-1/HK/5542404260727754259
10.681/3843504260727753702
10.610-3/5245604260727758509
10.610/3846304255942204221
10.610-1/HKM/4043404260727755461
10.680/I/5145304260727757922
10.683/50461004260727758479
10.610-3/BIND/5646604255942203446
10.681/4448604255942203194
10.610/4343304255942202029
10.610-1/HK/4242404255942203682