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.

Kissen zur Dekubitusprophylaxe — 404 UDI-DI variants, MDR

MD Atlas
Moritz Reha-Hilfen GmbH

Data from EUDAMED, last updated May 23, 2026

Kissen zur Dekubitusprophylaxe

426072775004A6

404 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: 426072775004A6
Device name: Kissen zur Dekubitusprophylaxe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 4, 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

404 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

basicUdiUlid01KNCT7KXBBB52X0HPM4K90R1M

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

10.619/485804260727755980
10.619/364604255942204733
10.619/445004260727757595
10.619/454304255942205518
10.619/404604260727755966
10.618-6/5043604260727757793
10.618-4/3840404255942201152
10.618-8/4543804255942201664
10.618-4/5343404255942201176
10.618-6/3842604255942200506
10.618-4/VB100/I/5041404255942202395
10.618-8/4246804255942205730
10.618-6/4643604255942200797
10.618-6/4447804255942200483
10.618-4/VB100/5042404255942203514
10.618-8/5043804255942205792
10.618-6/3844604260727757601
10.618-8/VB100/5243804255942204542
10.618-6/VB100/4343604255942200247
10.618-6/4343604260727757014
10.618-8/VB100/4247804255942204511
10.618-10/54461004255942203927
10.618-5/VB100/I/5540504255942202401
10.618-6/4843604260727758288
10.618-4346804255942200933