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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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Xen PA — 2 UDI-DI variants, MDR (Getinge Disinfection AB)

MD Atlas
Getinge Disinfection AB

Data from EUDAMED, last updated May 31, 2026

Xen PA

7340153700198H

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Getinge Disinfection AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7340153700198H
Device name: Xen PA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Getinge Disinfection AB
SRN: SE-MF-000001012
Country: Sweden
Email: info.disinfektion@getinge.com
Phone: +46 10 335 9800

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSQC73SQEM6VVQVA5N1MADR6

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

603600990107340153711778
603601060107340153711785