FDA Registration Active 🇫🇷 France

IDMED

Reg #: 3012072872 · FEI: 3012072872 · Expires 2026
Products
3
Proprietary Names
4
Establishment Types
1
Classifications
3

Registration Details

Registration Name
IDMED
Registration Number
3012072872
FEI Number
3012072872
Status
Active
Expiry Year
2026
Initial Importer
No
Address
3 rue John Maynard Keynes
City
Marseille Bouches-du-Rhone
Country
FR

Regulatory Submissions

510(k) Number
K243339

Owner / Operator

Firm Name
Idmed
Operator Number
10058016
Address
3 rue John Maynard Keynes
City
Marseille
State
Bouches-du-Rhone
Postal Code
13013
Country
FR
Correspondent
Frederic Bernert

US Agent

Business Name
IDMED Corp.
Contact Name
Remi Pourchier
Address
401 E Sonterra boulevard, Ste 375
City
San Antonio
State
TX
ZIP
78258
Country
US
Phone
210 7938941

Products

Device Name Product Code
Stimulator, Nerve, Peripheral, Electric KOI
Pupillometer, Ac-Powered HLG
Cuff, Tracheal Tube, Inflatable BSK

Proprietary Names

WiTOF ToFscan NeuroLight CuffGuard

Establishment Types

Manufacture Medical Device