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LUMENX MODEL GAT-577 PHOTOCOAGU. PULSED DYE LASER

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ALARIS® PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FRN·May 17, 2017

ON-Q PAIN PUMP

FDA Adverse Event
Other ·I-FLOW CORP.·Product code MEB·October 15, 2010

NEXIVA 18 GA X 1-1/4 IN SINGLE PORT

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 26, 2020

HEA 1.2 BEADCHIP KIT, SLIDE

FDA Adverse Event
Malfunction ·BIOARRAY SOLUTIONS LTD.·Product code PEP·August 16, 2021

ACUVUE® OASYS® 1-DAY FOR ASTIGMATISM WITH HYDRALUXE¿ TECHNOLOGY

FDA Adverse Event
Injury ·JOHNSON & JOHNSON VISION CARE - IRELAND·Product code LPL·April 11, 2026

MASUNAGA since 1905

FDA UDI
MASUNAGA OPTICAL MFG.CO.,LTD.·04582647307675·

SYMBIQ SINGLE CHANNE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 11, 2014

SYMBIQ SINGLE CHANNEL

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·January 30, 2014

PLM APL V13.4 ABG

FDA Adverse Event
Malfunction ·HOSPIRA, INC.·Product code FRN·April 2, 2009

OMNIPOD INSULIN PUMP

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·August 20, 2008

EXPRESSBRAID 10PK BLUE/WHITE

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS·Product code HTD·May 24, 2016

PLM APL V13.4 ABG

FDA Adverse Event
Malfunction ·HOSPIRA, INC.·Product code FRN·April 2, 2009

ALARIS PUMP MODULE ADMINISTRATION SET

FDA Adverse Event
Injury ·CAREFUSION CORPORATION·Product code FPA·April 16, 2014

CADD MEDICATION CASSETTES

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·April 28, 2022

UNICEL DXI 600 ACCESS® IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code MMI·October 15, 2011

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·November 21, 2019

SURESCAN

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 12, 2015

CADD EXTENSION SETS

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·April 28, 2022

PROTECTA XT CRT-D

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012