47 results
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55ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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SLIDEPREP PLUS CYTOLOGY CENTRIFUGE
FDA Adverse Event
Malfunction
·SEPARATION TECHNOLOGY, INC.·Product code JQC·December 19, 2012
SLIDEPREP PLUS CYTOLOGY CENTRIFUGE
FDA Adverse Event
Malfunction
·SEPARATION TECHNOLOGY, INC. PART OF THERMO FISHER SCIENTIFIC·Product code IFB·August 16, 2012
CLEAR-CRIT PLASTIC CAPILLARY TUBES
FDA Adverse Event
Malfunction
·SEPARATION TECHNOLOGY, INC.·Product code GIO·October 28, 1999
STAT-60
FDA Adverse Event
Malfunction
·SEPARATION TECHNOLOGY, INC.·Product code JQC·November 8, 2002
VANISHPOINT
FDA Adverse Event
Malfunction
·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·December 11, 2015
8.5F SHEATH WITH CURVE VIZ MDC
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·April 8, 2019
RESONANCE TECHNOLOGY INC.
FDA Adverse Event
Other
·RESONANCE TECHNOLOGY INC.·Product code LNH·July 25, 2006
SLIDEPREP PLUS CYTOLOGY CENTRIFUGE
FDA Adverse Event
Malfunction
·SEPARATION TECHNOLOGY, INC., PART OF THERMO FISHER SCIENTIFIC·Product code JQC·May 1, 2013
SLIDEPREP PLUS CYTOLOGY CENTRIFUGE
FDA Adverse Event
Malfunction
·SEPARATION TECHNOLOGY, INC., PART OF THERMO FISHER SCIENTIFIC·Product code JQC·August 30, 2012
PREMILENE NON-CARDIOVASCULAR
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAW·February 19, 2018
AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC
FDA Adverse Event
Malfunction
·NORTHGATE TECHNOLOGIES, INC·Product code FFK·June 29, 2022
AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC
FDA Adverse Event
Malfunction
·NORTHGATE TECHNOLOGIES, INC·Product code FFK·June 29, 2022
CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ MEDIUM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DYB·April 4, 2019
AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC
FDA Adverse Event
Injury
·NORTHGATE TECHNOLOGIES, INC·Product code FFK·March 17, 2022
AUTOLITH TOUCH 1.9FR PROBE, 375CM DS BSC
FDA Adverse Event
Injury
·NORTHGATE TECHNOLOGIES, INC·Product code FFK·March 17, 2022
CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH -
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DYB·April 16, 2019
INTELISWAB COVID-19 RAPID TEST
FDA Adverse Event
Malfunction
·ORASURE TECHNOLOGIES INC.·Product code QKP·January 6, 2022
AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC
FDA Adverse Event
Malfunction
·NORTHGATE TECHNOLOGIES, INC·Product code FFK·June 29, 2022
HIP PROSTHESIS COBALT + CHROMIUM METAL ON METAL
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECH. INC.·Product code KWA·September 7, 2014
WEBSTER CS CATHETER WITH AUTO ID TECHNOLOGY
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DRF·May 9, 2025