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

10.640/5644504260727758707
10.642/I/42451004255942206317
10.641/5643804255942204788
10.642/60481004255942207789
10.641/4244804260727758387
10.642/44441004260727753177
10.641/I/3840804255942208441
10.642/I/44401004255942204306
10.640/4346504260727753153
10.641/I/4242804255942206454
10.640/3939504255942217801
10.642/45431004260727753191
10.641/3840804260727759148
10.640/3441504255942217931
10.640/5646504260727753504
10.640/RS/4036504255942206331
10.642/I/HK/41411004255942206737
10.642/HK5/43431004255942200360
10.642/42541004255942201985
10.640/4842504260727753306
10.641/4343804260727753122
10.640/RS/5346504255942202517
10.641/4240804260727758981
10.641/RS/4646804255942204245
10.640/HK5/4646504260727756932