9 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Terragene Bionova(R) SCBI (BT220, BT221, BT222, BT223), Terragene Bionova (R) PCD (PCD220-C, PCD220-2, PCD222-C, PCD222-2), and Terragene Bionova(R) IC10/20FR Reader Incubator
FDA 510(k)
FDA Class 2
·General Hospital
INTELLIVUE MX40 PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
OPTI
FDA 510(k)
FDA Class 1
·Dental
BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 26, 2019
GMK-HINGE FIXED TIBIAL INSERT SIZE 2/23MM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code KRO·June 14, 2017
MONOPOLAR CURVED SCISSORS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·June 11, 2013
SPEEDBAND SUPERVIEW SUPER 7, MODELS 4204
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code MND·July 15, 2011
ASCENSIA CONTOUR
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·September 9, 2008
Medacta GMK HINGE, Tibial Insert Fixed, SIZE 2, HEIGHT 23 mm, REF 02.09.0223H, STERILE EO
FDA Enforcement
Class II
·Terminated·Medacta Usa Inc·July 12, 2017