535 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFICATIONS TO EXPEDIUM SPINE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Control Units
FDA UDI
Baxter Medical Systems GmbH + Co. KG·00887761975699·Footswitch TTH
FORAMATRON V, MODEL D680
FDA 510(k)
FDA Unclassified
·Unknown
STEAM STERILIZATION INTERGRATOR
FDA 510(k)
FDA Class 2
·General Hospital
5.0MM FLEXIBLE SHAFT
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HTO·April 29, 2013
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code FPA·May 9, 2011
ONE TOUCH ULTRASMART METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·July 24, 2008
PRECISION NOVI?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·June 26, 2025
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·July 20, 2011
OT ULTRA METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·April 3, 2012
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 27, 2011
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 3, 2012
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·October 6, 2010
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·June 1, 2011
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·September 16, 2010
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 19, 2012
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 22, 2010
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 30, 2010
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·September 2, 2011
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 12, 2011