50 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OCTAFIX OCCIPITAL CERVICAL PLATING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PAQ.210X140X170.BIONET CARDIO XP (EU ve
FDA UDI
AB MEDICA GROUP, S.A.·08428763010494·
ROLLO 210X30X16I.FK(SAUDI)
FDA UDI
AB MEDICA GROUP, S.A.·08428763005605·
Humeral Cup Stability
FDA UDI
FX SOLUTIONS·03701037309407·HUMERAL CUP STABILITY PE/TA6V Ø32/+9
TMA - Archwire
FDA UDI
ORMCO CORPORATION·00889989024654·ARCH LO-FRICT.TMA LO 17 X25 PK/10
Humeris Shoulder
FDA UDI
FX SOLUTIONS·03701037304457·TRIAL HUMERIS STEM T09
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193106991·HA PEEK EVOS Straight, ,9mmx8mmx 26mm , BICONVE...
Single Use Biliary Stent V
FDA UDI
OLYMPUS MEDICAL SYSTEMS CORP.·04953170186271·Single Use Biliary Stent V
RANDOX C-REACTIVE PROTEIN
FDA 510(k)
FDA Class 2
·Immunology
WHITE MTA MATERIAL
FDA 510(k)
FDA Class 2
·Dental
T.W. POWER SUPPLY
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code HQO·March 20, 2013
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 16, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·March 26, 2008
TUFTEX OVER-THE-WIRE EMBOLECTOMY CATHETER
FDA Adverse Event
Malfunction
·LEMAITRE VASCULAR, INC.·Product code DXE·November 8, 2023
TUFTEX OVER-THE-WIRE EMBOLECTOMY CATHETER
FDA Adverse Event
Malfunction
·LEMAITRE VASCULAR, INC.·Product code DXE·November 21, 2023
TUFTEX OVER-THE-WIRE EMBOLECTOMY CATHETER
FDA Adverse Event
Malfunction
·LEMAITRE VASCULAR, INC.·Product code DXE·September 15, 2023
TUFTEX OVER-THE-WIRE EMBOLECTOMY CATHETER
FDA Adverse Event
Malfunction
·LEMAITRE VASCULAR, INC.·Product code DXE·January 4, 2024
TUFTEX OVER-THE-WIRE EMBOLECTOMY CATHETER
FDA Adverse Event
Malfunction
·LEMAITRE VASCULAR, INC.·Product code DXE·January 4, 2024
TUFTEX OVER-THE-WIRE EMBOLECTOMY CATHETER
FDA Adverse Event
Malfunction
·LEMAITRE VASCULAR, INC.·Product code DXE·January 4, 2024
TUFTEX OVER-THE-WIRE EMBOLECTOMY CATHETER
FDA Adverse Event
Malfunction
·LEMAITRE VASCULAR, INC.·Product code DXE·January 11, 2024