9 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LUKENS 2-0 BRAIDED SILK SUTURES
FDA 510(k)
FDA Class 2
·Cardiovascular
INSPIRE 8 HOLLOW FIBER OXYGENATOR WITH INTEGRATED HARDSHELL VENOUS/CARDIOTOMY RESERVOIR
FDA 510(k)
FDA Class 2
·Cardiovascular
Gunther Tulip Vena Cava Filter Retrieval Set
FDA 510(k)
FDA Class 2
·Cardiovascular
AIMING ARM FOR RETRO SPIRAL BLADE LCKNG
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code FZX·April 26, 2021
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010
NEXGEN MIS STEMMED TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER INC·Product code JWH·January 11, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HLTHCARE CORP·Product code FRN·February 5, 2014
GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET
FDA Adverse Event
Malfunction
·COOK INC·Product code MMX·August 20, 2024
GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET
FDA Adverse Event
Malfunction
·COOK INC·Product code MMX·November 18, 2024