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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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Baldus Analog O2-N2O Mixer for… — 2 UDI-DI variants, MDR

MD Atlas
Baldus Sedation GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Baldus Analog O2-N2O Mixer for Analgesia 50

426063579ANALOG9J

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: Baldus Sedation GmbH & Co. KG

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 426063579ANALOG9J
Device name: Baldus Analog O2-N2O Mixer for Analgesia 50
Device model: Baldus Analog
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Baldus Sedation GmbH & Co. KG
SRN: DE-MF-000006223
Country: Germany
Email: info@baldus-sedation.de
Phone: +49 261 963892666

Variants by status

UDI-DI variants

2 UDI-DI variants

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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
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Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

16009-5004260635790639
16009-6004260635790066