17 results
·
51ms
·
Sources: EU EUDAMED, US FDA
PRO-TECH INTERNATIONAL
FDA registration
PRO-TECH INTERNATIONAL·7 products·🇺🇸 United States
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·February 14, 2024
UNICEL® DXC 600 PRO SYNCHRON® CHEMISTRY ANALYZER
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code JJE·December 27, 2010
GE/MARQUETTE
FDA Adverse Event
Malfunction
·MARQUETTE·Product code DRT·August 29, 2001
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code LIT·November 20, 2015
KYOCERA MEDICAL TECHNOLOGIES, INC
FDA Adverse Event
Malfunction
·KYOCERA MEDICAL TECHNOLOGIES, INC.·Product code OVE·April 5, 2024
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·February 5, 2016
ARCTIC SUN® 5000
FDA Adverse Event
Malfunction
·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·September 22, 2023
KOMAS Medical Technology GmbH
Authorized representative
🇩🇪 Germany·66 Manufacturers
Y. Sung Handelsvertretung
Authorized representative
🇩🇪 Germany·80 Manufacturers
Wellkang Ltd
Authorized representative
259 Manufacturers·3500 Devices
Lotus NL B.V.
Authorized representative
🇳🇱 Netherlands·584 Manufacturers·21427 Devices
Advena Limited
Authorized representative
🇲🇹 Malta·467 Manufacturers·13717 Devices
SUNGO Europe B.V.
Authorized representative
🇳🇱 Netherlands·1571 Manufacturers·20390 Devices
Sungo Cert GmbH
Authorized representative
🇩🇪 Germany·173 Manufacturers·3269 Devices
Obelis s.a.
Authorized representative
🇧🇪 Belgium·546 Manufacturers·18515 Devices
CMC Medical Devices & Drugs SL
Authorized representative
🇪🇸 Spain·698 Manufacturers·11260 Devices