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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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Medical Baths — 2 UDI-DI variants, MDR (ArjoHuntleigh AB)

MD Atlas
ArjoHuntleigh AB

Data from EUDAMED, last updated May 30, 2026

Medical Baths

5060693520044VT

2 UDI-DI variants

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

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

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 5060693520044VT
Device name: Medical Baths
Device model: AL21000-EU
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: ArjoHuntleigh AB
SRN: SE-MF-000000696
Country: Sweden
Email: info@arjo.com
Phone: +46 10 335 4500

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KJQSDP7R1S1VBW4TYF9FBJQT

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

AP02801EU101105055982712026
AP32211GB210105055982716420