34 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Hamilton-C6
FDA 510(k)
FDA Class 2
·Anesthesiology
HAMILTON-C6
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·February 10, 2025
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116023158·DMTL SmartFlex 270 High Energy Reusable (5X)
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116023172·DMTL SmartFlex 600 High Energy Reusable (5X)
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116023189·DMTL SmartFlex 1000 High Energy Reusable (5X)
CODMAN
FDA UDI
Cerenovus, Inc.·10886704001515·CODMAN SLIM-LINE Aneurysm Clip Bayonet Blade Le...
Life Instruments
FDA UDI
Life Instrument Corporation·M93072016580SFC0·S-Lift Cobb, 16mm
Life Instruments
FDA UDI
Life Instrument Corporation·M93072016580C0·Custom Cobb 16"7" handle 1/2
Accuvue+
FDA 510(k)
FDA Class 2
·Radiology
WATERLASE MD TURBO PLUS MODEL 7200XXX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 29, 2025
RESOLUTE INTEGRITY RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·July 14, 2017
ONYX
FDA Adverse Event
Injury
·MEDTRONIC COVIDIEN·Product code MFE·July 5, 2016
PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD
FDA Adverse Event
Death
·COVIDIEN·Product code FGE·July 14, 2017
PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD
FDA Adverse Event
Injury
·COVIDIEN·Product code FGE·July 14, 2017
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011
ISOLINE
FDA Adverse Event
Injury
·SORIN GROUP ITALIA SRL·Product code MRM·June 28, 2013
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014
ONYX
FDA Adverse Event
Injury
·MEDTRONIC COVIDIEN·Product code MFE·July 5, 2016
ONYX
FDA Adverse Event
Injury
·MEDTRONIC COVIDIEN·Product code MFE·July 5, 2016