7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
FIBRELIGHT NASAL SPECULA
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PROFEMUR LX HIP STEM
FDA 510(k)
FDA Class 3
·Orthopedic
EndoChoice Water Bottle Cap System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HANAULUX 2000
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FTD·April 3, 2014
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 5, 2010
UNKNOWN DEPUY ASR FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·December 3, 2012
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