6 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODEL 508 PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Anesthesiology
ASC QUADPORT + LAPAROSCOPIC ACCESS DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AI100 with Shonit
FDA 510(k)
FDA Class 2
·Hematology
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 17, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·February 6, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010