44 results · 30ms · Sources: EU EUDAMED, US FDA

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ARIES SARS-COV-2 EUA

FDA Adverse Event
Malfunction ·LUMINEX CORPORATION·Product code QJR·April 19, 2022

ARIES SARS-COV-2 EUA

FDA Adverse Event
Malfunction ·LUMINEX CORPORATION·Product code QJR·October 19, 2022

ARIES SARS-COV-2 EUA

FDA Adverse Event
Malfunction ·LUMINEX CORPORATION·Product code QJR·October 27, 2022

8010047-1996-00007

FDA Adverse Event
Malfunction ·Product code FDT·November 27, 1996

8010047-1996-00004

FDA Adverse Event
Malfunction ·Product code LQC·November 1, 1996

8010047-1997-00003

FDA Adverse Event
Malfunction ·Product code KOG·January 20, 1997

8010047-1997-00004

FDA Adverse Event
Malfunction ·Product code KOG·January 20, 1997

8010047-2015-00056

FDA Adverse Event
Malfunction ·January 19, 2015

8010047-2018-00346

FDA Adverse Event
Malfunction ·March 1, 2018

8010047-2018-00571

FDA Adverse Event
Malfunction ·April 3, 2018

AXSYM DIGOXIN III

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·March 8, 2011

ARIES SARS-COV-2 ASSAY

FDA Adverse Event
Malfunction ·LUMINEX CORPORATION·Product code QJR·May 21, 2021

THUNDERBEAT 5MM 20CM INLINE GRI

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GEI·May 2, 2014

VIDEO SYSTEM CENTER

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·November 19, 2021

ARIES SARS-COV-2 ASSAY (24 CASSETTES) - IVD

FDA Adverse Event
Malfunction ·LUMINEX CORPORATION·Product code QJR·February 1, 2023

ARIES SARS-COV-2 EUA

FDA Adverse Event
Malfunction ·LUMINEX CORPORATION·Product code QJR·October 27, 2021

ARIES SARS-COV-2 ASSAY (24 CASSETTES) - IVD

FDA Adverse Event
Malfunction ·LUMINEX CORPORATION·Product code QJR·May 26, 2023

ARIES SARS-COV-2 EUA

FDA Adverse Event
Malfunction ·LUMINEX CORPORATION·Product code QJR·August 16, 2022