8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
VR NETSERVE
FDA 510(k)
FDA Class 1
·Radiology
CoaguChek XS Plus System
FDA 510(k)
FDA Class 2
·Hematology
WG-SURGICAL SUTURES WITH NEEDLE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CELL-DYN 3700 SL ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 22, 2019
LCP ONE-THIRD TUBULAR PLATE WITH COLLAR 7 HOLES/81MM
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·December 21, 2020
LIGASURE IMPACT
FDA Adverse Event
Malfunction
·COVIDIEN LP·Product code GEI·June 20, 2014
DEPUY ASR FEM IMPLANT SZ 45
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·February 27, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·February 7, 2011