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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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WiTOF Sensor — 2 UDI-DI variants, MDR (Idmed)

MD Atlas
Idmed

Data from EUDAMED, last updated May 19, 2026

WiTOF Sensor

3665023WiTOF-SensorG5

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: Idmed

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3665023WiTOF-SensorG5
Device name: WiTOF Sensor
Device model: WiTOF-Sensor
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Idmed
SRN: FR-MF-000002402
Country: France
Email: info@idmed.fr

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K97TGQVE6CWVD8JR15SWTHP4

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

WiTOF-S03665023000559
WiTOF-FS03665023000573