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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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Sturzmatten ohne Alarmfunktion — 5 UDI-DI variants, MDR

MD Atlas
Moltoplast GmbH

Data from EUDAMED, last updated May 23, 2026

Sturzmatten ohne Alarmfunktion

9006018MOMASTUL

5 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: Moltoplast GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 9006018MOMASTUL
Device name: Sturzmatten ohne Alarmfunktion
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 23, 2022

Manufacturer & authorised representative

Manufacturer

Name: Moltoplast GmbH
SRN: AT-MF-000004503
Country: Austria
Email: med@moltoplast.com
Phone: +43 512 585407

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01GJFKHE61FNTR7GGEMKB5P2ZY

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

XMOMAT123AFNÖ90060183200560
650100123390060183200492
650100123290060183200324
650100123190060183200256
650100123090060183200188