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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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Endorectal probe — 2 UDI-DI variants, MDR (EDAP TMS FRANCE)

MD Atlas
EDAP TMS FRANCE

Data from EUDAMED, last updated May 19, 2026

Endorectal probe

3661690SONDEFO7M

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: EDAP TMS FRANCE

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Device characteristics

Active device

Clinical investigations

Registered: No

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 3661690SONDEFO7M
Device name: Endorectal probe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Oct 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: EDAP TMS FRANCE
SRN: FR-MF-000002207
Country: France
Email: serviceAR@edap-tms.com
Phone: +33 472 153 150

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K776GW0JAX3DN2259QKV1V26

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

Endorectal probe03661690000342
Endorectal probe03661690000205