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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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Diagnostic Ultrasound System — 2 UDI-DI variants, MDR (SternMed GmbH)

MD Atlas
SternMed GmbH

Data from EUDAMED, last updated May 23, 2026

Diagnostic Ultrasound System

42517308010KV

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: SternMed GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 42517308010KV
Device name: Diagnostic Ultrasound System
Device model: Sonos 10 / Sonos 12
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 29, 2022

Manufacturer & authorised representative

Manufacturer

Name: SternMed GmbH
SRN: DE-MF-000015421
Country: Germany
Email: info@sternmed.de
Phone: +49 757 35978 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G0CC74KWCN7SZ4FTSRE8P5ET

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

100106004251730800408
100104004251730800392