31 results
·
47ms
·
Sources: EU EUDAMED, US FDA
UNFO MED LTD.
FDA registration
UNFO MED LTD.·1 product·🇮🇱 Israel
BREEZE / TRANQUILCARE
FDA Adverse Event
Malfunction
·ARJOHUNTLEIGH, A BRANCH OF ARJO LTD MED AB·Product code FNM·March 12, 2013
ALPHA RELIEF
FDA Adverse Event
Malfunction
·ARJOHUNTLEIGH, A BRANCH OF ARJO LTD MED AB·Product code FNM·January 22, 2014
FLOWTRON EXCEL
FDA Adverse Event
Injury
·ARJOHUNTLEIGH·Product code JOW·December 15, 2011
TEMPO
FDA Adverse Event
Malfunction
·ARJO MED AB LTD·Product code FSA·November 1, 2013
MARISA
FDA Adverse Event
Other
·ARJO MED AB LTD.·Product code FSA·April 14, 2011
MARISA
FDA Adverse Event
Malfunction
·ARJO MED AB LTD.·Product code FSA·July 6, 2012
MAXILIFT
FDA Adverse Event
Malfunction
·ARJO MED AB LTD·Product code FSA·November 15, 2012
TEMPO
FDA Adverse Event
Injury
·ARJO MED AB LTD·Product code FSA·September 27, 2011
Q CORE SAPPHIRE EPIDURAL INFUSION PUMP
FDA Adverse Event
Malfunction
·Q CORE MEDICAL LTD·Product code FRN·May 21, 2015
STREAMLINE CONTINENTAL B
FDA Adverse Event
Malfunction
·HUNTLEIGH HEALTHCARE LTD - AKRON·Product code FNL·September 1, 2011
MARISA
FDA Adverse Event
Injury
·ARJO MED AB LTD·Product code FSA·June 15, 2011
TEMPO
FDA Adverse Event
Malfunction
·ARJO MED AB LTD.·Product code FSA·April 26, 2011
MAXILIFT
FDA Adverse Event
Malfunction
·ARJO MED AB LTD.·Product code FSA·April 1, 2011
OPERA
FDA Adverse Event
Malfunction
·ARJO MED AB, LTD.·Product code FSA·January 23, 2012
TEMPO
FDA Adverse Event
Malfunction
·ARJO MED AB LTD·Product code FSA·May 23, 2012
9617604-2007-00049
FDA Adverse Event
Malfunction
·Product code JOH·November 7, 2007
MARISA
FDA Adverse Event
Malfunction
·ARJO MED AB LTD.·Product code FSA·May 18, 2011
MARISA
FDA Adverse Event
Malfunction
·ARJO MED AB LTD.·Product code FSA·May 4, 2011
Q CORE SAPPHIRE EPIDURAL INFUSION PUMP
FDA Adverse Event
Malfunction
·Q CORE MEDICAL LTD·Product code FRN·May 21, 2015