8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BIVONA FLEXTEND PEDIATRIC & NEONATAL TRACHEOSTROMY TUBES
FDA 510(k)
FDA Class 2
·Anesthesiology
PORTEX® BIVONA® AIRE-CUF® NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code JOH·March 28, 2017
PORTEX®BIVONA® UNCUFFED NEONATAL AND PEDIATRIC TRACHEOSTOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD INC.,·Product code JOH·June 28, 2016
MODEL TT25RF
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CORRECTED-V.P.S.
FDA 510(k)
FDA Class 2
·Dental
ISERT ASPHERIC INTRAOCULAR LENS
FDA Adverse Event
Malfunction
·HOYA SURGICAL OPTICS, INC.·Product code HQL·December 6, 2010
REM 2000 35X80 DARTEX NO FB
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code IKY·February 5, 2013
COREVALVE 31MM AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 18, 2014