12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ALMA LASERS ALEX755 MODULE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036209360·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450212592·
GE LOGIQ 700
FDA 510(k)
FDA Class 2
·Radiology
ADC QS/IPD WORKSTATION
FDA 510(k)
FDA Class 2
·Radiology
BE-VKMO 70000 #QUADR-I HMO70000+VHK7100
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015
BE-VKMO 70000 #QUAD-I HMO70000+VHK7100
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015
BE-VKMO 70000 #QUADR-I HMO70000+VHK7100
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015
BE-VEMO 7000 #QUADR-I HMO70000+VHK7100
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015
1.8MM VA LOCKING BUTTRESS PIN W/T8 STARDRIVE RECESS/20MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·May 2, 2013
TRI TS FEMUR SZ6 LEFT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·September 15, 2014
CONVECTIVE PATIENT WARMER
FDA Adverse Event
Malfunction
·STRYKER CORP DBA GAYMAR·Product code DWJ·April 19, 2011