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.

Sitzkissen zur Dekubitusprophylaxe — 290 UDI-DI variants, MDR

MD Atlas
Werkmeister GmbH + Co. KG

Data from EUDAMED, last updated May 23, 2026

Sitzkissen zur Dekubitusprophylaxe

4048486113901YX

290 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: Werkmeister GmbH + Co. KG

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: 4048486113901YX
Device name: Sitzkissen zur Dekubitusprophylaxe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Werkmeister GmbH + Co. KG
SRN: DE-MF-000005120
Country: Germany
Email: info@werkmeister-gmbh.de
Phone: +49 (0) 5655 98 99 0

Variants by status

UDI-DI variants

290 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

basicUdiUlid01K4D4YYY41D7PKRYS0Q84G5H4

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

11015043604048486051938
11043838304048486053864
11043838304048486053840
11043838404048486053888
11043838404048486053918
11043838504048486053932
11043838504048486053956
11043838604048486054007
11043838604048486053970
11044040304048486054052
11044040304048486054021
11044040404048486054076
11044040404048486054090
11044040504048486054113
11044040504048486054144
11044040604048486054199
11044040604048486054168
11044043304048486054212
11044043304048486054236
11044043404048486054281
11044043404048486054250
11044043504048486054304
11044043504048486054328
11044043604048486054366
11044043604048486054342