12 results
·
57ms
·
Sources: EU EUDAMED, US FDA
FINE COMPANY LTD.
FDA registration
FINE COMPANY LTD.·1 product·🇯🇵 Japan
VITEK MS INSTRUMENT
FDA Adverse Event
Malfunction
·BIOMERIEUX, SA·Product code QBN·June 1, 2021
BEBACK CROSSING CATHETER
FDA Adverse Event
Malfunction
·BENTLEY INNOMED GMBH·Product code PDU·November 21, 2025
INDWELLING CATHETER
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code KNX·May 15, 2023
ACCENT XL
FDA Adverse Event
Injury
·ALMA LASERS LTD·Product code GEI·June 28, 2018
AUTOCAT 2
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL LLC·Product code DSP·September 16, 2022
TSI Quality Services
Authorized representative
🇩🇰 Denmark·34 Manufacturers·381 Devices
International Associates Auditing & Certification Limited
Authorized representative
🇮🇪 Ireland·46 Manufacturers·161 Devices
KHANG BAO INTERNATIONAL KFT
Authorized representative
🇭🇺 Hungary·119 Manufacturers·1262 Devices
CMC Medical Devices & Drugs SL
Authorized representative
🇪🇸 Spain·698 Manufacturers·11260 Devices
MedPath GmbH
Authorized representative
🇩🇪 Germany·537 Manufacturers·13464 Devices
MedEnvoy Global BV
Importer
🇳🇱 Netherlands·234 Manufacturers