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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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ToFscan AMG Sensor — 9 UDI-DI variants, MDR (Idmed)

MD Atlas
Idmed

Data from EUDAMED, last updated May 19, 2026

ToFscan AMG Sensor

3665023TOF-SensorNX

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: Idmed

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3665023TOF-SensorNX
Device name: ToFscan AMG Sensor
Device model: TOF-Sensor
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 7, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K9EX56E1W26J62YEKNKT3JHJ

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

TOF-FS03665023000061
TOF-ES03665023000078
TOF-ES_B03665023000504
TOF-S2_B03665023000498
TOF-PS2_B03665023000450
TOF-S203665023000047
TOF-FS_B03665023000511
TOF-PS_B03665023000481
TOF-PS03665023000054