140 results · 33ms · Sources: EU EUDAMED, US FDA

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MULLINS-X PTV CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

UltrOx

FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436123157·UltrOx High Level Disinfectant

WEC-7101A POCKET SIZE ECG MONITOR AND ACCESSORIES

FDA 510(k)
FDA Class 2 ·Cardiovascular

VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT

FDA 510(k)
FDA Class 2 ·Dental

GMK-REVISION FEMUR REVISION PS SIZE 6 RIGHT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 12, 2017

GMK-HINGE FIXED TIBIAL TRAY SIZE 3 R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·August 28, 2019

GMK HINGE FEMUR SIZE 5 RIGHT

FDA Adverse Event
Injury ·MEDACTA INTERNAIONAL SA·Product code KRO·August 21, 2014

GMK-REVISION FIXED TIBIAL TRAY CEMENTED SIZE 3 RIGHT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 25, 2017

GMK-REVISION FEMUR REVISION PS SIZE 3

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 19, 2019

GMK HINGE FEMUR SIZE 2 RIGHT

FDA Adverse Event
Injury ·Product code KRO·September 12, 2014

GMK REVISION TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 29, 2025

GMK-REVISION FEMUR REVISION PS SIZE 6 L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 6, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020

LIGASURE

FDA Adverse Event
Injury ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018