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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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Sonostat — 2 UDI-DI variants, MDR (gbo Medizintechnik AG)

MD Atlas
gbo Medizintechnik AG

Data from EUDAMED, last updated May 30, 2026

Sonostat

426036481B010XH

2 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: gbo Medizintechnik AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426036481B010XH
Device name: Sonostat
Device model: Sonostat touch 133
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: gbo Medizintechnik AG
SRN: DE-MF-000018065
Country: Germany
Email: info@gbo-ag.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KS5JABZ31HFDM5QP97JSNJD0

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

032-0-300004260364810103
032-0-310004260364812114