16 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Flexible Overtube
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PROPELLER HEAD SCREW SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304270268·
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101032·JAEGER LID PLATE STAINLESS STEEL
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100974·DESMARRES LID RETRACTOR #2
BD NEXIVA CLOSED IV CATHETER SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES
FDA 510(k)
FDA Class 2
·Anesthesiology
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code JOH·November 18, 2010
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code BTR·December 9, 2010
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code BTR·February 1, 2011
COREVALVE 31MM AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·October 17, 2014
6000 CMS
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·June 11, 2013
HUDSON CONCHATHERM NEPTUNE HEATED HUMIDIFIER
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTT·July 8, 2011
BD NEXIVA¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·Product code FOZ·June 25, 2021
PEN NDL 32G 4MM PRO 100 BOX 1200 US
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMI·July 30, 2021
BD NANO¿ 2ND GEN PEN NEEDLES 32G X 4MM (100 COUNT)
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·October 25, 2023
BD PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·February 23, 2021