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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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Bezüge für Schüttflexible… — 90 UDI-DI variants, MDR (Moltoplast GmbH)

MD Atlas
Moltoplast GmbH

Data from EUDAMED, last updated May 23, 2026

Bezüge für Schüttflexible Lagerungssysteme

9006018INLFUESF

90 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: 9006018INLFUESF
Device name: Bezüge für Schüttflexible Lagerungssysteme
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

90 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJJ3EMM7D2CFB20T26P6H3W1

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

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XSIB885040PUNL90060182208826
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XSB88504090060182201100
XSB885145PUNL90060182201896
XSB885422PUNL90060182204002
XSB885540PUNL90060182204866
XSB8999990060182207768
XSB88514590060182201728
XSB88502090060182200356
XSB885423PUNL90060182204248
XSB885100PUNL90060182201414
XSB885350PUNL90060182203012

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