8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
HGB-CONTROL SET/MULTIPLE
FDA 510(k)
FDA Class 2
·Hematology
SUSPENSION 7
FDA 510(k)NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 9, 2014
KEEPSAFE FALL MONITOR
FDA Adverse Event
Malfunction
·DONGGUAN POSEY MEDICAL DEVICE LTD.·Product code KMI·November 3, 2010
OBTAPE TRANSOBTURATOR SLING
FDA Adverse Event
Injury
·MENTOR WORLDWIDE LLC·Product code FTL·December 21, 2012
GYC-1000
FDA Adverse Event
Malfunction
·NIDEK CO., LTD.·Product code HQF·June 18, 2015
Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system
FDA Enforcement
Class I
·Terminated·CareFusion 303, Inc.·August 12, 2020