586 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFICATION TO CD HORIZON SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Entuit Thrive
FDA UDI
XERIDIEM MEDICAL DEVICES, INC.·00827002356177·Entuit Gastrostomy BR Balloon Retention Feeding...
MODIFICATION TO LIPOPROTEIN (A) SPQ III ANTIBODY REAGENT SET
FDA 510(k)
FDA Class 2
·Immunology
NORMED EXTREMITY TITANIUM HAND AND SMALL FRAGMENT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 8, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 23, 2011
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
JUMAO - JM - E. CHINA·Product code IOR·August 27, 2014
OT ULTRAMINI
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 1, 2010
OT ULTRA EASY METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 3, 2012
OT ULTRAMINI
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 7, 2010
OT ULTRA EASY METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 14, 2012
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·June 3, 2011
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 2, 2011
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 11, 2011
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 20, 2012
OT ULTRAMINI
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 23, 2010
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·July 5, 2011
OT ULTRAMINI
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 6, 2011
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 27, 2011
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 31, 2012