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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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CliniMat — 63 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

4056538MAT005LY

63 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4056538MAT005LY
Device name: CliniMat
Device model: Klinikmatratzen Prophylaxe/Therapie
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

63 UDI-DI variants

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Applied filters

basicUdiUlid01GPDERFFW097VJNK8ZS7QTQXQ

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

KM4626304056538007000
KM4004004056538004771
KM4859804056538008069
KM4859904056538008076
KM4860004056538008083
KM4860104056538008090
KM4626404056538007017
KM4004104056538004788
KM3695404056538003989
SO-KM5089804056538009028
KM4860204056538008250
SO-KM5049804056538008717
KM4836004056538007802

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