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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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hup DES FORTE M — 3 UDI-DI variants, MDR

MD Atlas
Hagleitner Hygiene International GmbH

Data from EUDAMED, last updated May 23, 2026

hup DES FORTE M

900835321984BG

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Hagleitner Hygiene International GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 900835321984BG
Device name: hup DES FORTE M
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 19, 2024

Manufacturer & authorised representative

Manufacturer

Name: Hagleitner Hygiene International GmbH
SRN: AT-MF-000023685
Country: Austria
Email: christian.rasser@hagleitner.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HVTF5SR3MJ4SERT3KGQJD584

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

170162709008353223245
44503045425509008353219910
44503045420009008353219842