542 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VERITAS COLLAGEN MATRIX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65810629151·CLEAR INTRAORAL ELASTICS 5/16" 4 OZ X-HEAVY
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040116880·CLEAR INTRAORAL ELASTICS 5/16" 4 OZ X-HEAVY
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037313541·STABILITY TRIAL CUP FOR BOACH Ø32 +15
STANDARD ...
Sklar®
FDA UDI
SKLAR CORPORATION·10649111155802·SCALPEL HANDLE #3L
FLEXIBLE OCCLUSION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
DINAMAP PRO 1000 MONITOR, MODEL 1000
FDA 510(k)
FDA Class 2
·Cardiovascular
ACRYSOF TORIC
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./ HUNTINGTON·Product code HQL·April 12, 2013
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 21, 2011
WALLSTENT ENTERAL ENDOPROSTHESIS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC IRELAND, LTD·Product code MQR·June 19, 2008
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