10,000 results
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90ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·February 19, 2010
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·March 10, 2010
COBAS 6000 C501MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code KQG·January 29, 2010
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·March 10, 2010
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·February 11, 2010
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·April 7, 2010
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·May 19, 2010
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·April 7, 2010
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·May 24, 2010
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·April 7, 2010
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·April 7, 2010
MEDICAL LABORATORY AUTOMATION
FDA Adverse Event
Injury
·MEDICAL LABORATORY AUTOMATION·Product code KQG·September 5, 1996
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORPORATION·Product code KQG·November 15, 2010
HEMOCHRON RESPONSE, 110V
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·December 17, 2009
HEMOCHRON RESPONSE COAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·October 16, 2009
SYSMEX CA-1000
FDA Adverse Event
Malfunction
·TOA MEDICAL ELECTRONICS·Product code KQG·November 17, 1995
ACL 3000
FDA Adverse Event
Other
·INSTRUMENTATION LABORATORIES, INC.·Product code KQG·October 21, 1995
HEMOCHRON ACT MONITOR
FDA Adverse Event
Malfunction
·ITC·Product code KQG·June 23, 2006
HEMOCHRON RXDX SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·September 10, 2009
HEMOCHRON RESPONSE SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code KQG·September 10, 2009