8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
GODDE T-TUBE BLUE SILICONE TYMPANOSTOMY TUBE
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209121687·
IBA PROTON THERAPY SYSTEM-PROTEUS 235
FDA 510(k)
FDA Class 2
·Radiology
Owl Night Guard
FDA 510(k)
FDA Unclassified
·Unknown
M3150 INFORMATION CENTER LOCAL DATABASE
FDA Adverse Event
Death
·PHILIPS MEDICAL SYSTEMS·Product code MHX·May 23, 2014
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code IOR·December 3, 2012
SYSTEM 5 SINGLE TRIGGER ROTARY HANDPIECE
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·September 29, 2010
Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.
FDA Enforcement
Class II
·Terminated·STERILMED, INC.·December 16, 2015