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.

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

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: 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

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

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

XSB885025PUNL90060182200806
XSB88503590060182200974
XSB88578090060182205160
XSB885526PUNL90060182204620
XSB885900PUNL90060182205610
XSB88524690060182202190
XSB88557090060182204934
XSB88526590060182202572
XSB885260PUNL90060182202404
XSB88541890060182203326
XSB885780PUNL90060182205238
XSB88590090060182205542
XSB88684090060182206914
XLSOBEZUGBEINLAGRUNGPUNL90060182209052
XSB885997PUNL90060182206464
XSB99998PUNL90060182208444
XSB885570PUNL90060182205092
XSB899998PUNL90060182207904
XSB88685090060182207140
XSB885020PUNL90060182200424
XSB885418PUNL90060182203494
XSB885265PUNL90060182202640
XSB88504PUNL90060182201278
XSB885800PUNL90060182205474
XSB885420PUNL90060182203876

1 2 3 4