30 results
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41ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Non-contact Infrared Body Thermometer, Model HTD8808C, HTD8818A, HTD8816C
FDA 510(k)
FDA Class 2
·General Hospital
LIGHTSPEED ULTRA COMPUTED TOMOGRAPHY SYSTEM WITH WIDE-VIEW
FDA 510(k)
FDA Class 2
·Radiology
MEDITHERM MED2000
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
BD ARTERIAL CANNULA 20G/45MM
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FOZ·December 22, 2023
MAVERICK2 MONORAIL PTCA CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·October 15, 2008
ENRHYTHM DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code DXY·August 11, 2011
VG CR MONO-LCK BRG 10X71
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·July 2, 2013
LIFEPAK 20
FDA Adverse Event
Malfunction
·MEDTRONIC EMERGENCY RESPONSE SYSTEMS·Product code LDD·March 2, 2009
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 2, 2024
CLINITEST RAPID COVID-19 ANTIGEN TEST
FDA Adverse Event
Malfunction
·HEALGEN SCIENTIFIC LLC·Product code QKP·November 10, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·July 7, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 9, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·August 17, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 1, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·July 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·August 4, 2022