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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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hygienicDES FORTE MED — 4 UDI-DI variants, MDR

MD Atlas
Hagleitner Hygiene International GmbH

Data from EUDAMED, last updated May 23, 2026

hygienicDES FORTE MED

900835321981BA

4 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: 900835321981BA
Device name: hygienicDES FORTE MED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 24, 2025

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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HWCHA2XZVXZVDHRFBJAET48Y

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

44601019081409008353230526
44601019087309008353230540
44601019085509008353224822
44601019080009008353224808