188 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AARON A950 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A950 ELECTROSURGICAL GENERATOR, 240V
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DUCKWORTH & KENT, LTD.
FDA registration
DUCKWORTH & KENT, LTD.·20 products·🇬🇧 United Kingdom
HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED
FDA 510(k)
FDA Class 2
·Orthopedic
BRIDGE FX
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SETROX S 60
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVN·March 26, 2013
STENOSCOP
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD.·Product code JAA·February 25, 2011
FORTIFY DR, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·August 19, 2014
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 16, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 11, 2010
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 23, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 9, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 18, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 16, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 2, 2012
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·October 5, 2010
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 10, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 17, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 2, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 14, 2011
OT ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·June 6, 2011