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Merit Medical Systems, Inc.

Manufacturer
🇺🇸 United States·8 Importers

Merit Medical Systems, Inc.

Manufacturer
🇺🇸 United States·2 Importers

MERIT MEDICAL SYSTEMS, INC

FDA registration
MERIT MEDICAL SYSTEMS, INC·14 products·🇺🇸 United States

Merit Medical Systems, Inc.

FDA registration
Merit Medical Systems, Inc.·3 products·🇺🇸 United States

MERIT MEDICAL SYSTEMS, INC.

FDA registration
MERIT MEDICAL SYSTEMS, INC.·122 products·🇺🇸 United States

Merit Medical Systems, Inc.

FDA registration
Merit Medical Systems, Inc.·15 products·🇺🇸 United States

MERIT MEDICAL SYSTEMS, INC., GUIDE WIRE TORQUE DEVICE

FDA 510(k)
FDA Class 2 ·Cardiovascular

FLUID ADMINISTRATION SETS

FDA Adverse Event
Other ·MERIT MEDICAL SYSTEMS, INC.·Product code FPA·April 17, 2008

FLUID ADMINISTRATION SETS

FDA Adverse Event
Other ·MERIT MEDICAL SYSTEMS, INC.·Product code FPA·April 17, 2008

FLUID ADMINISTRATION SETS

FDA Adverse Event
Other ·MERIT MEDICAL SYSTEMS, INC.·Product code FPA·April 17, 2008

FLUID ADMINISTRATION SETS

FDA Adverse Event
Other ·MERIT MEDICAL SYSTEMS, INC.·Product code FPA·April 17, 2008

FLUID ADMINISTRATION SETS

FDA Adverse Event
Other ·MERIT MEDICAL SYSTEMS, INC.·Product code FPA·April 17, 2008

FLUID ADMINISTRATION SETS

FDA Adverse Event
Other ·MERIT MEDICAL SYSTEMS, INC.·Product code FPA·April 17, 2008

FLUID ADMINISTRATION SETS

FDA Adverse Event
Other ·MERIT MEDICAL SYSTEMS, INC.·Product code FPA·April 17, 2008

FLUID ADMINISTRATION SETS

FDA Adverse Event
Other ·MERIT MEDICAL SYSTEMS, INC.·Product code FPA·April 17, 2008

MERIT MEDICAL SYSTEMS INC.

FDA Adverse Event
Injury ·MERIT MEDICAL SYSTEMS INC.·Product code DRE·August 22, 2016

MERIT MEDICAL SYSTEMS INC.

FDA Adverse Event
Death ·MERIT MEDICAL SYSTEMS INC.·Product code DTL·November 6, 1997

PRELUDE SHORT SHEATH INTRODUCER IN CUSTOM KIT

FDA Adverse Event
Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DYB·April 16, 2009

PRELUDE SHORT SHEATH INTRODUCER IN CUSTOM KIT

FDA Adverse Event
Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DYB·April 16, 2009

ESOPHYX Z+

FDA Adverse Event
Injury ·ENDOGASTRIC SOLUTIONS INC·Product code ODE·August 27, 2024