Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

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

XS88524690060182101424
XSI88096590060182105552
XS88542290060182102346
XSI88091590060182105248
XS88515590060182101288
XS88534090060182101738
XSI88682090060182105866
XS88686090060182104562
XS88599790060182103886
XSI88626090060182105620
XSIUNIVERALKISSEN90060182106160
XSI88681890060182105798
XS88685090060182104258
XS88500490060182100120
XS88590090060182103404
XS88526090060182101592
XS885422490060182102414
XS88542390060182102582
XSI88095690060182105316
XS885100290060182100984
XS88504090060182100670
XS88541890060182102032
XS899999990060182104944
XS88510090060182100816
XS88578090060182103268

1 2 3