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.

CliniMat — 6 UDI-DI variants, MDR (SOFTLINE-Schaum GmbH & Co. KG)

MD Atlas
SOFTLINE-Schaum GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

CliniMat

4056538MAT004LW

6 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: SOFTLINE-Schaum 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: 4056538MAT004LW
Device name: CliniMat
Device model: Klinikmatratzen Standard
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 10, 2023

Manufacturer & authorised representative

Manufacturer

Name: SOFTLINE-Schaum GmbH & Co. KG
SRN: DE-MF-000014549
Country: Germany
Email: info@softline-schaum.de
Phone: +493367840770

Variants by status

UDI-DI variants

6 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

basicUdiUlid01GPDENESBWY9CV00F7CATZCC9

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

KM4626104056538006980
KM3698804056538004641
KM4626004056538006973
KM4856904056538007918
KM4815704056538007871
KM4856804056538007901