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CUSTOM DEFINED PRODUCT

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES DR·Product code DXO·October 21, 2014

OPUS

FDA Adverse Event
Malfunction ·DORNIER MEDIZINTECHNIK GMBHH·Product code KQS·January 18, 2002

FR2

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS, HEARTSTREAM·Product code MKJ·July 13, 2010

HEARTSTART ONSITE

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·December 28, 2011

HEARTSTART ONSITE

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·December 29, 2011

HEARTSTRING ONSITE

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·December 29, 2011

CHARITE ENDPLATE SIZE UNKNOWN

FDA Adverse Event
Malfunction ·DEPUY SPINE, INC.·Product code MJO·April 11, 2006

WAVELIGHT FS200 FEMTOSECOND LASER

FDA Adverse Event
Injury ·WAVELIGHT GMBH·Product code OOE·September 1, 2015

INTERA 3000

FDA Adverse Event
Malfunction ·INTERA ONCOLOGY·Product code LKK·December 16, 2022

MAGNA PURE LC INSTRUMENT

FDA Adverse Event
Malfunction ·PRECISION SYSTEMS SCIENCES·Product code JJE·November 12, 2004

V60 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·August 16, 2017

PERI-GUARD

FDA Adverse Event
Injury ·BIO-VASCULAR, INC.·Product code FTL·December 13, 1996

HANDPIECE MICS

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·January 13, 2023

TRULIGN TORIC POSTERIOR CHAMBER IOL

FDA Adverse Event
Injury ·BAUSCH + LOMB·Product code MJP·June 12, 2015

CRYSTALENS ACCOMMODATING IOL

FDA Adverse Event
Injury ·BAUSCH + LOMB·Product code NAA·June 12, 2015

CRYSTALENS ACCOMMODATING IOL

FDA Adverse Event
Injury ·BAUSCH + LOMB·Product code NAA·December 20, 2016

CRYSTALENS HD IOL

FDA Adverse Event
Injury ·BAUSCH + LOMB·Product code NAA·May 23, 2012

CRYSTALENS

FDA Adverse Event
Injury ·BAUSCH + LOMB·Product code NAA·July 20, 2011

EVIS EXERA III DUODENOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDT·April 20, 2026

HEARTSINE SAMARITAN 200P AND PAD PAK

FDA Adverse Event
Malfunction ·HEARTSINE TECHNOLOGIES, LTD CANBERRA HOUSE·Product code MKJ·January 23, 2015