13 results
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31ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MEMSCAP AS
FDA registration
MEMSCAP AS·1 product·🇳🇴 Norway
Pressure dome - 30034
FDA UDI
Memscap AS·07071977000082·
SP 840 - 32021
FDA UDI
Memscap AS·07071977000075·
EDWARDS AQUARIUS SYSTEM
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code KDI·January 30, 2009
CABLE,XDUCER,IBP,MEMSCAP,6PIN
FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904003870·
CABLE,XDUCER,IBP,MEMSCAP,12PIN
FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904003887·
WOLFE ARTHROSCOPY SCOPE
FDA Adverse Event
Injury
·UNKNOWN·Product code HRX·August 1, 2009
ELECTRO SHOCK MACHINE
FDA Adverse Event
Death
·Product code GXC·April 2, 2011
EAKIN COHESIVE SEALS
FDA Adverse Event
Injury
·CONVATEC·Product code EZR·February 13, 2013
STOMAHESIVE STRIPS
FDA Adverse Event
CONVATEC·Product code EZR·February 13, 2013
UNSPECIFIED BD POLYCARBONATE SYRINGE
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FMF·August 30, 2019
FMC CASSETTE
FDA Adverse Event
Injury
·ERIKA DE REYNOSA, S.A. DE C.V.·Product code FKX·September 16, 2019
SPECTRA OPTIA
FDA Adverse Event
Malfunction
·TERUMO BCT·Product code LKN·September 10, 2019