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

10.642/49441004255942201107
10.640/4643504260727753245
10.640/4443504260727753160
10.642/I/44441004255942208403
10.640/4048504260727759131
10.642/RS/50461004255942207734
10.642/46441004255942202593
10.642/50491004255942207710
10.641/6045804255942204177
10.642/43431004260727753108
10.640/HK5/4943504260727756987
10.642/50431004260727753436
10.640/RS/4340504255942202777
10642/56481004260727753511
10.640/4835504255942201510
10.640/RS/5046504255942202500
10.641/5649804260727757960
10.640/4046504260727757748
10.641/4242804255942217924
10.641/4043804255942217870
10.642/46461004260727753269
10.640/3838504255942204863
10.640/4543504260727753207
10.640/HK5/4643504260727756970
10.640/5846504255942201374

3 4 5 6 7