21 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Ultra ICE Plus PI 9 MHz Peripheral Imaging Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Halyard
FDA UDI
Avanos Medical, Inc.·10680651928488·HYH,UBLOCK,UBT,-,-,10
AVANOS
FDA UDI
Avanos Medical, Inc.·00193493928484·AVANOS* Universal Block Trays
Cranial Guidance Software
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613327538328·Cranial Guidance Sales Demo
Arena-L®
FDA UDI
SPINEFRONTIER, INC.·00190361038979·Rasp Trial Head, 38X28 Lordotic 8°, 17L
Arena-L®
FDA UDI
SPINEFRONTIER, INC.·00190361038931·Rasp Trial Head, 38X28 Lordotic 8°, 9L
Arena-L®
FDA UDI
SPINEFRONTIER, INC.·00190361038948·Rasp Trial Head, 38X28 Lordotic 8°, 11L
Arena-L®
FDA UDI
SPINEFRONTIER, INC.·00190361038955·Rasp Trial Head, 38X28 Lordotic 8°, 13L
Arena-L®
FDA UDI
SPINEFRONTIER, INC.·00190361038962·Rasp Trial Head, 38X28 Lordotic 8°, 15L
ENDOSKELETON® TA
FDA UDI
TITAN SPINE, LLC·00191375051329·7 Deg Lordotic, Implant Caddy, Base, Large
ENDOSKELETON® TA
FDA UDI
TITAN SPINE, LLC·00191375051336·7 Deg Lordotic, Implant Caddy, Base, X-Large
ENDOSKELETON® TA
FDA UDI
TITAN SPINE, LLC·00191375051305·7 Deg Lordotic, Implant Caddy, Base, Standard
MICROTHERMX-100 MICROWAVE ABLATION SYSTEM AND ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BLADEVIEW
FDA 510(k)
FDA Class 2
·Radiology
OSSURE LOEP KIT
FDA Adverse Event
Death
·AGNOVOS HEALTHCARE USA, LLC·Product code MQV·December 27, 2018
OSSURE LOEP KIT
FDA Adverse Event
Death
·AGNOVOS HEALTHCARE USA, LLC·Product code MQV·January 18, 2020
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·June 20, 2013
TERUMO ADVANCED PERFUSION SYSTEM 1
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·July 1, 2011
HEARTSTRING II PROXIMAL SEAL SYSTEM
FDA Adverse Event
Malfunction
·GUIDANT CARDIAC SURGERY·Product code DXC·September 29, 2008
CHROMID® CARBA SMART
FDA Adverse Event
Malfunction
·BIOMERIEUX S.A.·Product code JSO·August 23, 2018