411 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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C-CURVE Interbody Fusion Device
FDA 510(k)
FDA Class 2
·Orthopedic
BCI
FDA UDI
ICU MEDICAL, INC.·10610586040689·
R & D 4K RETIC
FDA 510(k)
FDA Class 2
·Hematology
MIPAL
FDA 510(k)
FDA Class 2
·Cardiovascular
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
SCREWS
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·October 29, 2014
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 9, 2011