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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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Voluson Expert 18, Voluson Expert 20,… — 8 UDI-DI variants, MDR

MD Atlas
GE Healthcare Austria GmbH & Co OG

Data from EUDAMED, last updated May 23, 2026

Voluson Expert 18, Voluson Expert 20, Voluson Expert 22

8406821BUG00372HL

8 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: GE Healthcare Austria GmbH & Co OG

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 8406821BUG00372HL
Device name: Voluson Expert 18, Voluson Expert 20, Voluson Expert 22
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 20, 2023

Manufacturer & authorised representative

Manufacturer

Name: GE Healthcare Austria GmbH & Co OG
SRN: AT-MF-000001461
Country: Austria
Email: eudamed@gehealthcare.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HAS03TJSWCV48HC9TKHTZRA5

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

Voluson Expert 18 BT2400195278699800
Voluson Expert 18 BT25 00195278770226
Voluson Expert 20 BT25 00195278770158
Voluson Expert 22 BT2500195278770271
VolusonExp BT24 to BT25 UPG00195278814685
Voluson Expert 20 BT2400195278699824
Voluson Expert 22 BT2400195278699848
Voluson Exp to BT24 UPG00195278677587