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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 kit — 2 UDI-DI variants, MDR (Idmed)

MD Atlas
Idmed

Data from EUDAMED, last updated May 19, 2026

TOFscan kit

3665023TF2-SystemC3

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: 3665023TF2-SystemC3
Device name: TOFscan kit
Device model: TF2-System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 24, 2026

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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Applied filters

basicUdiUlid01KPZXZAY4MZJ9GAMZ96WX1VN0

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

TF2-KIT03665023001433
TF2-KIT-EMG_RU03665023002850