10 results
·
47ms
·
Sources: EU EUDAMED, US FDA
HORIZON XL PATIENT MONITOR
FDA Adverse Event
Malfunction
·MENNEN MEDICAL, INC.·Product code MHX·February 13, 1995
HORIZON XL PATIENT MONITOR
FDA Adverse Event
MENNEN MEDICAL INC.·Product code DRT·May 23, 1997
SYNCHRONOUS DEFIBRILLATOR
FDA Adverse Event
Injury
·MENNEN MEDICAL, INC.·Product code LDD·December 13, 1993
DEFIBRILLATOR MONITORING SCREEN
FDA Adverse Event
Injury
·MENNEN MEDICAL, INC.·Product code LDD·January 5, 1996
AdQuipment medical b.v.
Importer
🇳🇱 Netherlands·7 Manufacturers
VEROMED SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
Importer
🇵🇱 Poland·9 Manufacturers
NATECH
Importer
🇫🇷 France·11 Manufacturers
CEpartner4U
Authorized representative
🇳🇱 Netherlands·160 Manufacturers·5787 Devices
PROYECTOS HOSPITALARIOS INTERNACIONAL, S.A
Importer
🇪🇸 Spain·23 Manufacturers
GEENEN PANCREATIC STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·October 1, 2020