84 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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QUICKIE 2 WHEELCHAIR
FDA Adverse Event
Malfunction
·QUICKIE DESIGNS INC.·Product code IOR·November 19, 1996
ANSPACH X MAZ
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code ERL·October 17, 2014
MEZ BREATHE ATOMIZER
FDA Adverse Event
Malfunction
·HEALTH & LIFE (SUZHOU) CO., LTD.·Product code CCQ·November 5, 2013
TEEX/8-3 MHZ
FDA Adverse Event
Malfunction
·SONOSITE,INC.·Product code IYO·January 11, 2012
OAS 450 MHZ SERVER
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code JQP·November 24, 2003
SONICATH 3.2F, 20 MHZ
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code ITX·June 20, 2007
OAS 400 MHZ WORKSTATION
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code JTC·March 13, 2003
ACCELERATOR APS CENTRIFUGE MODULE
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code JQP·February 18, 2014
LAP/12-5 MHZ TRANSDUCER
FDA Adverse Event
Malfunction
·SONOSITE,INC.·Product code ITX·February 23, 2007
TEE/8-3 MHZ TRANSDUCER
FDA Adverse Event
Malfunction
·SONOSITE, INC.·Product code IYO·February 17, 2009
TEE/8-3 MHZ TRANSDUCER
FDA Adverse Event
Malfunction
·SONOSITE, INC.·Product code IYO·September 12, 2008
TEE/8-3 MHZ TRANSDUCER
FDA Adverse Event
Malfunction
·SONOSITE, INC.·Product code IYO·September 12, 2008
91341 TELEMETRY TRANSMITTER, 1400 MHZ
FDA Adverse Event
Malfunction
·SPACELABS HEALTHCARE·Product code DSI·August 22, 2008
TEE/8-3 MHZ TRANSDUCER
FDA Adverse Event
Malfunction
·SONOSITE, INC.·Product code IYO·August 22, 2008
91341 TELEMETRY TRANSMITTER, 1400 MHZ
FDA Adverse Event
Malfunction
·SPACELABS HEALTHCARE·Product code DSI·August 22, 2008
91341 TELEMETRY TRANSMITTER, 1400 MHZ
FDA Adverse Event
Malfunction
·SPACELABS HEALTHCARE·Product code DRG·August 22, 2008
TEE/8-3 MHZ TRANSDUCER
FDA Adverse Event
Malfunction
·SONOSITE, INC.·Product code IYO·August 29, 2008
TEE/8-3 MHZ TRANSDUCER
FDA Adverse Event
Malfunction
·SONOSITE,INC.·Product code IYO·September 12, 2008
SONICATH ULTRA 3.2F 20 MHZ
FDA Adverse Event
Malfunction
·SCIMED, A DIVISION OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006
SONICATH ULTRA 3.2F 20 MHZ
FDA Adverse Event
Malfunction
·SCIMED, A DIVISION OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006