410 results · 26ms · Sources: EU EUDAMED, US FDA

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XSTAT 30 Pouch

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SIMPLICITY WINGED QD INFUSION SET

FDA 510(k)
FDA Class 2 ·General Hospital

TSRH SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ECHOTIP ULTRA ENDOBRONCHIAL HD ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·August 26, 2022

ECHOTIP PROCORE ENDOBRONCHIAL HD BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·January 16, 2024

ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·July 19, 2023

ECHOTIP ULTRA ENDOBRONCHIAL HD ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·July 26, 2022

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·June 29, 2023

ECHOTIP PROCORE ENDOBRONCHIAL HD BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·March 14, 2024

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·February 5, 2023

ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·April 9, 2024

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·February 7, 2023

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·June 22, 2023

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·May 19, 2023

ECHOTIP PROCORE ENDOBRONCHIAL HD BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·June 7, 2023

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·April 17, 2023

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·October 3, 2022

M2A MAGNUM PF CUP 48MM O.D. X 42MM I.D.

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 12, 2011

SENSATION? SHORT THROW

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code FDI·October 29, 2014

RIATA ST ACTIVE FIXATION

FDA Adverse Event
Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 8, 2013