8 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ORION'S URETHRAL CATHETERIZATION KIT WITH CATHETER AND BAG
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
F.T.I. MEDICAL LIGHT GUIDE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
OIL, MINERAL
FDA 510(k)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
UNIVERSAL DRIVER SHAFT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·February 5, 2013
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Injury
·ANIMAS CORP.·Product code LZG·December 21, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 18, 2014