10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
EBV(EPSTEIN-BARR VIRUS) TEST KIT
FDA 510(k)
FDA Class 1
·Microbiology
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994843036·TRAY 1854207 SOLERA X14I CROSSLINK INST
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209129324·
AiORTA - Plan v2.0
FDA 510(k)
FDA Class 2
·Radiology
PENPOINT, FLEXIBLE & SPOT MARKERS & RADOACTIVE RUL
FDA 510(k)MINICAP TRANSFER SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 6, 2020
MINICAP TRANSFER SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 3, 2023
COREVALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 6, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code MDS·October 5, 2010
RF3000 RADIOFREQUENCY GENERATOR
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEI·December 3, 2012