10,000 results · 420ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

D-TRONPLUS

FDA Adverse Event
Malfunction ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code L Z·September 17, 2004

IMP,TSV,4.1MM,SBM,13

FDA Adverse Event
Injury ·L·Product code DZE·August 15, 2023

L. ULTRA THIN CONDOMS

FDA Adverse Event
Injury ·L·Product code HIS·February 29, 2016

ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER DUAL LUMEN

FDA Adverse Event
Injury ·COVIDIEN L. L. C.·Product code FOS·December 4, 2015

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Malfunction ·CORDIS L L C (PR)·Product code NIQ·March 18, 2005

RENU MULTIPLUS SOLUTION

FDA Adverse Event
Other ·B+L·Product code LPN·April 6, 2011

RENU MULTIPLUS

FDA Adverse Event
Other ·B+L·Product code LPN·April 6, 2011

RENU MULTIPLUS

FDA Adverse Event
Other ·B+L·Product code LPN·April 6, 2011

RENU MULTIPLUS

FDA Adverse Event
Injury ·B+L·Product code LPN·April 6, 2011

RENU MULTIPLUS

FDA Adverse Event
Injury ·B+L·Product code LPN·April 6, 2011

RENU MULTIPLUS

FDA Adverse Event
Other ·B+L·Product code LPN·April 6, 2011

COBAS INTEGRA 800

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 15, 2008

ALINITY LACTATE DEHYDROGENASE2

FDA Adverse Event
Malfunction ·A.I.D.D LONGFORD·Product code CFJ·August 17, 2022

ACCU-CHEK ® PERFORMA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 4, 2010

COBAS 6000 C501 MODULE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·May 11, 2010

ALINITY C TOTAL BILIRUBIN REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code CIG·June 29, 2021

COBAS 6000 C501 MODULE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·May 19, 2008

ACCU-CHEK ® PERFORMA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 14, 2011

COBAS 6000 C501 MODULE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·August 12, 2008

CARBON DIOXIDE

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code KHS·November 15, 2021