7,121 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REUS,NK SPO2 SNSR,63",ADLT FNG CLP
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828187572·REUS,NK SPO2 SNSR,63",ADLT FNG CLP
REUS,NK SPO2 SNSR,39",PED FNG CLP
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828187602·REUS,NK SPO2 SNSR,39",PED FNG CLP
REUS,NK SPO2 SNSR,39",ADLT FNG CLP
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828187589·REUS,NK SPO2 SNSR,39",ADLT FNG CLP
REUS,NK SPO2 SNSR,63",PED FNG CLP
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828187596·REUS,NK SPO2 SNSR,63",PED FNG CLP
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·UNKNOWN·Product code FSA·November 8, 2013
KRAYENBUEHL HK FNG REST SML
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code GDG·October 8, 2003
EDM VENTRICULAR CATHETER, BARIUM IMPREGNATED, 35 CM
FDA Adverse Event
Injury
·MEDTRONIC NEUROSURGERY·Product code GWM·August 5, 2019
ENTROY
FDA Adverse Event
Malfunction
·ARJO HOSPITAL EQUIPMENT AB·Product code FNG·October 28, 2016
CLIP SLINGS
FDA Adverse Event
Malfunction
·MEDIBO MEDICAL PRODUCTS N.V.·Product code FNG·January 3, 2012
MEDCARE
FDA Adverse Event
Malfunction
·MEDCARE PRODUCTS·Product code FNG·February 21, 2012
VOYAGER
FDA Adverse Event
Malfunction
·ARJOHUNTLEIGH MAGOG·Product code FNG·March 2, 2012
VOYAGER
FDA Adverse Event
Malfunction
·ARJOHUNTLEIGH MAGOG, INC·Product code FNG·February 27, 2012
MAXI TWIN
FDA Adverse Event
Malfunction
·ARJO HOSPITAL EQUIPMENT AB·Product code FNG·March 20, 2012
HOYER PRESENCE LIFT WITH SCALE
FDA Adverse Event
Malfunction
·SR INSTRUMENTS·Product code FNG·March 27, 2012
MAXI SKY 600 CEILING LIFT
FDA Adverse Event
Malfunction
·ARJOHUNTLEIGH, INC·Product code FNG·January 13, 2012
VOYAGER
FDA Adverse Event
Injury
·ARJOHUNTLEIGH MAGOG·Product code FNG·February 24, 2012
MEDCARE
FDA Adverse Event
Other
·MEDCARE PRODUCTS·Product code FNG·February 15, 2012
HOYER HML-400 LIFT WITH HOYER SLING
FDA Adverse Event
Malfunction
·STARITE INTERNATIONAL, LTD.·Product code FNG·March 31, 2012
ERGOLIFT
FDA Adverse Event
Malfunction
·BHM MEDICAL, INC.·Product code FNG·February 8, 2009
8030916-2008-00058
FDA Adverse Event
Malfunction
·Product code FNG·January 28, 2009