26 results · 22ms · Sources: EU EUDAMED, US FDA

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TUOHY EPIDURAL NEEDLE

FDA 510(k)
FDA Class 2 ·Anesthesiology

BUSCH®, BNA®

FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120305621·Diamond, cone rounded edge, medium grit

APEX INTRAMEDULLARY NAIL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ALPHA DX SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

NEEDLE 27GA 1-1/2IN

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·July 26, 2019

C21617 DE LIFE SYSTEMS $PHISIO

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·October 24, 2013

ERBE

FDA Adverse Event
Malfunction ·LEONHARD LANG GMBH·Product code GEI·November 2, 2022

NEEDLE 27GA 1-1/2IN

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·July 16, 2019

ADMIRAL XTREME

FDA Adverse Event
Injury ·INVATEC SPA·Product code LIT·April 2, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 9, 2011

ACCU-CHEK SPIRIT CARTRIDGE

FDA Adverse Event
Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·April 15, 2008

CP82200 I MIRANDOLA

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·April 6, 2012

CP85341 FR PARIS

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

NEEDLE 27GA 1-1/2IN

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·April 23, 2020

ERBE

FDA Adverse Event
Malfunction ·LEONHARD LANG GMBH·Product code GEI·March 8, 2023

ERBE

FDA Adverse Event
Malfunction ·LEONHARD LANG GMBH·Product code GEI·February 18, 2025

EMORY/CL/KNNSTN ATLANTA GA1

FDA Adverse Event
Other ·SORIN GROUP USA·Product code DWF·August 19, 2010

DUKE UNIV DURHAM NC 1

FDA Adverse Event
Other ·SORIN GROUP USA, INC.·Product code DWF·July 15, 2011

ERBE

FDA Adverse Event
Injury ·LEONHARD LANG GMBH·Product code GEI·July 27, 2022

COBE REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC COATING

FDA Adverse Event
Death ·SORIN GROUP ITALIA SRL·Product code KFM·November 23, 2016