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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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Schüttflexible Lagerungssysteme — 61 UDI-DI variants, MDR

MD Atlas
Moltoplast GmbH

Data from EUDAMED, last updated May 23, 2026

Schüttflexible Lagerungssysteme

9006018SFLAYW

61 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: 9006018SFLAYW
Device name: Schüttflexible Lagerungssysteme
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 22, 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

61 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJFNBQ07FWQTJ6ZV83HPV9VH

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

XS88535090060182101806
XS88692790060182104630
XS88554090060182103022
XS88606090060182104012
XS88502390060182100366
XS885155390060182101356
XS88557090060182103190
XS9999890060182105002
XS88514590060182101110
XS885526590060182102896
XSI88682290060182105934

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