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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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Pflegebettmatratzen Therapie — 87 UDI-DI variants, MDR

MD Atlas
SOFTLINE-Schaum GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Pflegebettmatratzen Therapie

4056538MAT003LU

87 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: 4056538MAT003LU
Device name: —
Device model: Pflegebettmatratzen Therapie
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

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

87 UDI-DI variants

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Applied filters

basicUdiUlid01KRWZBD07SAKK521C2GEVDR46

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

SO-M2570404056538006287
SO-M3925504056538009295
SO-M5047504056538008694
SO-M2464804056538991125
SO-M4449704056538005648
SO-M2974004056538005938
M1773404056538998513
M1760804056538999503
M1868404056538999497
M1792304056538999404
M1868504056538995369
SO-M2366204056538993891

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