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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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Sonda ultradźwiękowa — 1 UDI-DI variant, MDD (Echo-Son SA)

MD Atlas
Echo-Son SA

Data from EUDAMED, last updated May 30, 2026

Sonda ultradźwiękowa

B-05904292005208

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Echo-Son SA

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Device characteristics

Active device

Legacy certificates

Certificate number: 5-824-200-1707
Type: refdata.legacy.mdd-certificate-type.ii-4
Notified body: NEOEMKI Nemzeti Orvostechnikai Eszköz Megfelelőségértékelő és Tanúsító Korlátolt Felelősségű Társaság (NEOEMKI LLC) (1011)
Validity: Jul 29, 2022

Identity & classification

Basic UDI-DI: B-05904292005208
Device name: Sonda ultradźwiękowa
Device model: S 255B
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Jan 11, 2022

Manufacturer & authorised representative

Manufacturer

Name: Echo-Son SA
SRN: PL-MF-000004830
Country: Poland
Email: info@echoson.eu
Phone: +48818863613

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01FN605DP2ZCQ594MZDZ05HER8

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

590429200520805904292005208