Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012072872

FEI Number

3012072872

Entity Name

IDMED

City/State/Country

Marseille Bouches-du-Rhone, FR

Establishment Address

3 rue John Maynard Keynes, Marseille Bouches-du-Rhone 13013, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Idmed (Owner Number: 10058016)

Owner / Operator Contact Address

3 rue John Maynard Keynes, Marseille, FR-13 13013, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

WiTOF ToFscan NeuroLight

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KOI	Stimulator, Nerve, Peripheral, Electric	Anesthesiology	Class 2	868.2775	2025-12-15
KOI	Stimulator, Nerve, Peripheral, Electric	Anesthesiology	Class 2	868.2775	2018-06-26
HLG	Pupillometer, Ac-Powered	Ophthalmic	Class 1	886.1700	2020-01-14

Official Correspondent

Frederic Bernert

US Agent Details

Remi Pourchier Business: IDMED Corp. Email: r.pourchier@idmed.fr Phone: (210) 7938941

Related Public Records

Same Entity

Idmed

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012072872. Last updated year: 2026. Please use registration number 3012072872 when referencing this establishment in official correspondence.