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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 CAPS — 5 UDI-DI variants, MDR

MD Atlas
Hagleitner Hygiene International GmbH

Data from EUDAMED, last updated May 23, 2026

hygienicDES CAPS

9008353114219L

5 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: 9008353114219L
Device name: hygienicDES CAPS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 30, 2022

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

5 UDI-DI variants

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Applied filters

basicUdiUlid01G6TBSVVSXM787SGGSDC45NB2

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

N.B4.14.01.01 / 44601014330609008353228899
44601013330009008353114215
44601014335509008353114239
44601014331409008353114222
44601014337309008353114246