44 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FUKUDA DENSHI DYNASCOPE MODEL DS-8100N/8100M PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Premium Surgiclip
FDA UDI
Covidien LP·10884521057548·Clip Applier
Alice 6
FDA UDI
Respironics, Inc.·00606959047112·Alice 6 Base Station, LDE with Masimo, INTL
RNK TELEPHONIC STETHOSCOPE, MODEL TR-1
FDA 510(k)
FDA Class 2
·Cardiovascular
VALVED TEARAWAY INTRODUCER GENERATION II
FDA 510(k)
FDA Class 2
·Cardiovascular
SURGICLIP
FDA Adverse Event
Injury
·COVIDIEN·Product code GDO·October 18, 2011
PREMIUM SURGICLIP S-9.0 TITANIUM
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY USSC PUERTO RICO·Product code FZP·January 27, 2014
PREMIUM SURGICLIP
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FZP·August 9, 2011
PREMIUM SURGICLIP S-9.0 TITANIUM
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY USSC·Product code FZP·January 27, 2014
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 30, 2025
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
UNKNOWN DEPUY CUP
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code KWY·May 29, 2013