7,378 results · 27ms · Sources: EU EUDAMED, US FDA

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Foxman Vitrectomy Lens Ring

FDA UDI
OCULAR INSTRUMENTS, INC.·00630238106641·

XPREZZON

FDA Adverse Event
Malfunction ·SPACELABS MEDICAL INC.·Product code MHX·October 2, 2013

REPLY

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code NVZ·October 2, 2015

CSF-VENTRICULAR CATHETER STANDARD 23 CM

FDA Adverse Event
Injury ·MEDTRONICS PS MEDICAL·Product code JXG·September 25, 1996

ASH SPLIT CATHETER

FDA Adverse Event
Malfunction ·MEDCOMP·Product code MPB·October 25, 2002

V-GO DISPOSABLE INSULIN DELIVERY DEVICE

FDA Adverse Event
Death ·ZEALAND PHARMA U.S. INC.·Product code LZG·November 30, 2020

ALIZEA

FDA Adverse Event
Malfunction ·MICROPORT CRM S.R.L.·Product code DXY·December 12, 2024

QUADRA ASSURA CRT-D QUAD RF HV

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·March 7, 2017

HEARTSINE SAMARITAN PAD 360P

FDA Adverse Event
Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·April 8, 2026

V-GO DISPOSABLE INSULIN DELIVERY DEVICE

FDA Adverse Event
Malfunction ·MANNKIND CORPORATION - V-GO·Product code LZG·September 26, 2023

V-GO DISPOSABLE INSULIN DELIVERY DEVICE

FDA Adverse Event
Malfunction ·ZEALAND PHARMA U.S. INC.·Product code LZG·August 10, 2021

HEARTSINE SAMARITAN PAD 350P

FDA Adverse Event
Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code NSA·May 20, 2026

HEARTSTART MRX - EMS DEFIBRILLATOR

FDA Adverse Event
Other ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 5, 2011

CAPSURE

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 1997

CAPSURE Z NOVUS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DXY·September 9, 2005

CAPSURE SP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 26, 1999

SIGMA 300 DR

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL, INC.·Product code DXY·July 11, 2001

MULTIFUNCTION ELECTRODE

FDA Adverse Event
Other ·CARDIOTRONICS SYSTEM, INC.·Product code LDD·May 22, 1995

THERMOFLOW FILTER PORT

FDA Adverse Event
Malfunction ·ARC MEDICAL·Product code BYD·October 27, 2009

ULTRAVIEW

FDA Adverse Event
SPACELABS HEALTHCARE·Product code DRT·June 12, 2013