22 results · 37ms · Sources: EU EUDAMED, US FDA

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INTRAVASCULAR ADMINISTRATION SET

FDA 510(k)
FDA Class 2 ·General Hospital

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772813834·GENUMEDI PRO SILVER SIZE III

RUSCH

FDA UDI
TELEFLEX INCORPORATED·34026704624080·

REFLECTION CONSTRAINED LINER

FDA 510(k)
FDA Class 2 ·Orthopedic

NEWPORT E360 VENTILATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

EASYSPINE SCREW, UNKOWN SIZE OR TYPE

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·August 17, 2020

UPHOLD VAGINAL SUPPORT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code OTP·April 1, 2016

UPHOLD VAGINAL SUPPORT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code OTP·April 1, 2016

UPHOLD VAGINAL SUPPORT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code OTP·April 1, 2016

UPHOLD VAGINAL SUPPORT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code OTP·April 1, 2016

ACRYSOF

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·May 15, 2013

ENRHYTHM DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code DXY·June 13, 2011

PLUMSET WITH 0.2 MICRON FILTER AND CLAVE

FDA Adverse Event
Malfunction ·HOSPIRA DE COSTA RICA LTD.·Product code FPA·May 12, 2008

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE ROD, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE ROD, UNKNOWN

FDA Adverse Event
Malfunction ·LDR MEDICAL·Product code NKB·March 24, 2020

EASYSPINE SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·LDR MÉDICAL·Product code NKB·July 9, 2019