Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

LINEAR-ARRAY TRANSCUTANEOUS ULTRASOUND… — 9 UDI-DI variants, MDR

MD Atlas
SONOSCANNER

Data from EUDAMED, last updated May 19, 2026

LINEAR-ARRAY TRANSCUTANEOUS ULTRASOUND PROBES

37011046LAUSPROBESWX

9 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: SONOSCANNER

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 37011046LAUSPROBESWX
Device name: —
Device model: LINEAR-ARRAY TRANSCUTANEOUS ULTRASOUND PROBES
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 30, 2024

Manufacturer & authorised representative

Manufacturer

Name: SONOSCANNER
SRN: FR-MF-000002220
Country: France
Email: qara@sonoscanner.com

Variants by status

UDI-DI variants

9 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01J6F72Z6A565RYAH12WYYSRZ5

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

PR1403701104600307
PR2503701104600369
PR2803701104600277
PR5103701104600062
PR5203701104600079
PR5703701104600130
PR6003701104600161
PR6203701104600420
PR9903701104600239