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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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Power supply for ToFscan & WiTOF — 8 UDI-DI variants, MDR (Idmed)

MD Atlas
Idmed

Data from EUDAMED, last updated May 19, 2026

Power supply for ToFscan & WiTOF

3665023TOFWiTOF-PSNB

8 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Idmed

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3665023TOFWiTOF-PSNB
Device name: Power supply for ToFscan & WiTOF
Device model: TOFWiTOF-PS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K97W6N157CNEVPWGP1F38DAD

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-CHAR_TI03665023000146
TOF-CHAR_C8_JP03665023000641
TOF-CHAR03665023000108
TOF-CHAR_US03665023000122
TOF-CHAR_C8_BR03665023000436
TOF-CHAR_C8_KR03665023000443
TOF-CHAR_C803665023000139
TOF-CHAR_UK03665023000115