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

10.610-1/4942404260727752507
10.610-2/3632504255942202340
10.681/5050504255942207390
10.610-3/5650604260727752729
10.610-2/4845404255942200513
10.681/4446504255942206119
10.680/3436304260727758011
10.610-2/I/4246504255942201718
10.610-2/4341504260727752200
10.610-1/HK5/4646404255942201213
10.610-2/4645504255942205006
10.610-2/I/4044504260727751647
10.683/44481004260727758158
10.610-2/HKM/3638504255942207932
10.610-2/BIND/4543504255942203309
10.610-1/5845404260727752750
10.610-2/RG60/I/4643504260727751708
10.610-2/4141504260727752156
10.610/5248804255942207963
10.610-5/4343504255942202715
10.610-2/4240504255942207871
10.610-2/BIND/4846504255942203477
10.610-2/BIND/5046504255942203460
10.610-1/BIND/3845404255942203392
10.610-1/4348404255942203224