175 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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