85 results · 75ms · Sources: EU EUDAMED, US FDA

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Well-Life Healthcare Limited

FDA registration
Well-Life Healthcare Limited·12 products·🇹🇼 Taiwan

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·September 17, 2009

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 16, 2009

OPTIFLOW + ADULT NASAL CANNULA

FDA Adverse Event
Death ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·March 2, 2022

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FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 6, 2009

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FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 10, 2009

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FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 10, 2009

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 4, 2019

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FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 2, 2011

VITALITY 2

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 3, 2013

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FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 10, 2009

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FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 9, 2009

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 9, 2009

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 10, 2009

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 9, 2009

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 10, 2009

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·November 9, 2009

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 26, 2010

CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·April 12, 2019

CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·May 8, 2019