52 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RT300 FES cycle ergometer
FDA 510(k)
FDA Class 2
·Neurology
WILDER LACRIMAL DILATOR
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896018495·WILDER LACRIMAL DILATOR SINGLE ENDED MEDIUM TIP #2
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L162470120·16mm H x 24mm W x 70mm L XLIF Trial 12 degree L...
2GC HIP/KNEE MODULAR SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020
LIGASURE
FDA Adverse Event
Injury
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 16, 2021
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MPRI·Product code NVY·October 10, 2014
HEARTSTART FRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 6, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 14, 2011