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

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Kerrison Rongeurs

FDA 510(k)
FDA Class 2 ·Neurology

AGC V2 TOTAL KNEE SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304242265·

COMFORT STANDING WHEELCHAIR, HERO SERIES

FDA 510(k)
FDA Class 2 ·Physical Medicine

MODIFICATION TO: VERTEX RECONSTRUCTION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

NOVOSYN QUICK UNDY 4/0(1,5)70CM DS16MDDP

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·January 24, 2020

ACCESS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·May 20, 2015

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 8, 2014

SPRINT QUATTRO SECURE S

FDA Adverse Event
Malfunction ·MPRI·Product code LWS·June 7, 2013

TERUMO CDI 500 BLOOD PARAMETER MONITOR

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP.·Product code DRY·June 24, 2011

NI

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 29, 2016

NOVOSYN VIOLET 4/0 (1,5)45CM DS19 (M)RCP

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·May 18, 2022

NOVOSYN VIOLET 4/0 (1,5)45CM DS19 (M)RCP

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·May 27, 2022

NI

FDA Adverse Event
Malfunction ·NI·Product code FPA·March 8, 2017

NI

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 24, 2016

NI

FDA Adverse Event
Malfunction ·NI·Product code FPA·March 8, 2017

NI

FDA Adverse Event
Malfunction ·NI·Product code FPA·March 8, 2017

NI

FDA Adverse Event
Malfunction ·NI·Product code FPA·March 8, 2017

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 6, 2021

NOVOSYN VIOLET 1 (4) 90CM HRT37S (M)

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·May 13, 2019

NOVOSYN VIOLET 0 (3.5) 70CM FR26 (M)

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·February 27, 2020