8 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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QBC III CENTRIFUGAL HEMATOLOGY SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756554138·CYSTOLOGY TRAY
LUNGPOINT PROCEDURE PLANNING
FDA 510(k)
FDA Class 2
·Radiology
VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0
FDA 510(k)
FDA Class 2
·Orthopedic
CAPIOX RX05
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·June 25, 2014
ACCU-CHEK ULTRAFLEX INFUSION SET
FDA Adverse Event
Injury
·DISETRONIC MEDICAL SYSTEMS·Product code LZG·October 22, 2008
UNKNOWN SCORPIO 5MM PATELLA COMPONENT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·November 4, 2010
BIOFIRE® BLOOD CULTURE IDENTIFICATION 2 (BCID2) PANEL
FDA Adverse Event
Malfunction
·BIOFIRE DIAGNOSTICS, LLC·Product code PAM·January 31, 2024