500 results · 43ms · Sources: EU EUDAMED, US FDA

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GenePOC GBS LB

FDA 510(k)
FDA Class 1 ·Microbiology

SOLITARIE PEEK ANTERIOR SPINAL SYSTEM-TO BE CALLED COLITAIRE 35

FDA 510(k)
FDA Class 2 ·Orthopedic

MP 719

FDA 510(k)
FDA Unclassified ·Unknown

BIODESIGN URETHRAL SLING

FDA Adverse Event
Injury ·COOK BIOTECH, INC.·Product code PAG·October 9, 2014

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 21, 2011

SENOMARK BREAST BIOPSY MARKER

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code NEU·May 28, 2013

Phoenix AP AST Indicator Bag, Catalog Number 246006

FDA Enforcement
Class II ·Terminated·Becton Dickinson & Co.·March 6, 2019

GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Death ·WILLIAM COOK EUROPE·Product code DTK·July 23, 2019

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·July 9, 2020

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·October 2, 2019

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·October 31, 2019

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·October 7, 2019

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·October 7, 2019

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·October 2, 2019

(17-0557) ANK C/X IMPL B17/D4.5/L17(IMPLANTS)

FDA Adverse Event
Injury ·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·June 17, 2021

GUNTHER TULIP NAVALIGN JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·February 5, 2021

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·December 5, 2019

AUTOPULSE® LIFEBAND

FDA Adverse Event
Malfunction ·ZOLL CIRCULATION·Product code DRM·February 4, 2022

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·September 9, 2020

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·April 21, 2020