13 results
·
93ms
·
Sources: EU EUDAMED, US FDA
HANDHELD DOPLER/PEN TRANSDUCER 3MHZ
FDA 510(k)
FDA Class 2
·Radiology
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209131112·
Arthrex®
FDA UDI
ARTHREX, INC.·00888867309616·LOW PROFILE SCREW, TI, 4.5 X 90MM
POWER PACK 160 SIEMENS-ELEMA AB
FDA 510(k)
FDA Class 2
·Anesthesiology
ACCUFLEX
FDA 510(k)
FDA Class 1
·Clinical Chemistry
BD SURGIPHOR¿ STERILE WOUND IRRIGATION SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code FQH·January 12, 2023
BD SURGIPHOR¿ STERILE WOUND IRRIGATION SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code FQH·January 12, 2023
FORTIFY ASSURA DR, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 6, 2014
SCREW
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·December 3, 2012
AUTOFEED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·September 9, 2010
BD SURGIPHOR - SURGIRINSE
FDA Adverse Event
Injury
·CAREFUSION, INC·Product code FQH·August 5, 2022
VANGUARD SSK PS TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·July 1, 2019
VANGUARD SSK FEMUR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·July 1, 2019