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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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S+ Probe, M+ Probe, XL+ Probe — 3 UDI-DI variants, MDR (Echosens)

MD Atlas
Echosens

Data from EUDAMED, last updated May 19, 2026

S+ Probe, M+ Probe, XL+ Probe

366226400000000000000086J

3 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: Echosens

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 366226400000000000000086J
Device name: S+ Probe, M+ Probe, XL+ Probe
Device model: Probes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Echosens
SRN: FR-MF-000003894
Country: France
Email: contact@echosens.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JJA1TE4WVDF4JJYEK9MERD42

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

XL+ Probe03662264000072
S+ probe03662264000065
M+ Probe03662264000058