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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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Biocleanse Ultra — 6 UDI-DI variants, MDR (Getinge Disinfection AB)

MD Atlas
Getinge Disinfection AB

Data from EUDAMED, last updated May 31, 2026

Biocleanse Ultra

73401537001487

6 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: Getinge Disinfection AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73401537001487
Device name: Biocleanse Ultra
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KSQCM4RKS3Q52DRYMFZ2VDME

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

DS202/507340153711518
DS012/TSINGLE07340153711556
DS012/T07340153711563
DS202/4X507340153711525
DS012/4X507340153711549
DS012/507340153711532