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

10.640/3442504255942200957
10.641/4252804255942202579
10.640/4949504260727753412
10.640/3646504255942217740
10.640/RS/4646504255942202258
10.641/4442804260727758905
10.642/HK5/46461004255942207154
10.640/I/4340504255942207703
10.654/303204260727757441
10.654/302404255942202319
10.654/404504260727755751
10.654/354504260727755638
10.654/403804260727755720
10.654/303004255942201527
10.654/403704260727755713
10.654/484504255942200759
10.654/424004260727755799
10.654/454004260727755867
10.654/455004255942202074
10.654/454304260727755874
10.654/434504260727759155
10.654/384004260727755690
10.654/545004260727755959
10.654/384504260727756864
10.654/454904255942200919