10,000 results · 45ms · Sources: EU EUDAMED, US FDA

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SELECTSECURE MRI SURESCAN

FDA Adverse Event
Malfunction ·MPRI·Product code NVN·May 20, 2022

ULTEGRA RPFA-TRAP

FDA Adverse Event
Malfunction ·ACCUMETRICS·Product code JOZ·June 22, 2000

ULTEGRA RPFA-TRAP

FDA Adverse Event
Malfunction ·ACCUMETRICS·Product code JOZ·May 3, 2000

SELECTSECURE MRI SURESCAN

FDA Adverse Event
Malfunction ·MEDTRONIC SINGAPORE OPERATIONS·Product code NVN·October 22, 2021

ULTEGRA RPFA-TRAP

FDA Adverse Event
Malfunction ·ACCUMETRICS·Product code JOZ·June 2, 2000

ULTEGRA RPFA-TRAP

FDA Adverse Event
Malfunction ·ACCUMETRICS·Product code JOZ·May 3, 2000

ULTEGRA RPFA-TRAP

FDA Adverse Event
Malfunction ·ACCUMETRICS·Product code JOZ·May 3, 2000

ULTEGRA RPFA-TRAP

FDA Adverse Event
Malfunction ·ACCUMETRICS·Product code JOZ·May 3, 2000

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·CORDIS LLC (PR)·Product code NIQ·October 20, 2005

SELECTSECURE MRI SURESCAN

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO VILLALBA·Product code NVN·July 18, 2025

DUETT PRO SEALING DEVICE

FDA Adverse Event
Injury ·VASCULAR SOLUTIONS, INC.·Product code MGB·August 20, 2003

CYPHER SIROLUMUS-ELUTING CORONARY STENT.

FDA Adverse Event
Death ·CORDIS LLC (PR)·Product code NIQ·June 30, 2005

INTERSTIM II

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·October 18, 2016

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code NIQ·October 20, 2005

TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC·Product code NIQ·July 22, 2005

BD SYRINGE 60ML LL BRAZIL

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·August 1, 2019

EXTRACORPOREAL FILTER

FDA Adverse Event
Injury ·PALL BIOMEDICAL PRODUCTS COMPANY·Product code LLB·January 21, 1995

AFRI MEDICAL SYNFLO CS 540

FDA Adverse Event
Injury ·AFRI MEDICAL CO·Product code LLB·February 10, 2006

EXTRACORPOREAL CUSTOM TUBING PACK

FDA Adverse Event
Death ·GISH BIOMEDICAL·Product code LLB·September 24, 1993

EXTRACORPOREAL SINGLE PATIENT SYSTEM

FDA Adverse Event
Death ·BAXTER-EXTRACORPOREAL MEDICAL SPECIALITIES, INC.·Product code LLB·August 9, 1993