35 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964069192·Endo Carry-On Procedure Kit
Endeavour™ TruColor™
FDA UDI
METREX RESEARCH, LLC·00810210820257·Endeavour™ TruColor™ headlight system - North A...
Sklar®
FDA UDI
SKLAR CORPORATION·10649111002854·E-Z LOCK INSTR STRINGER 5X12"
Drill Stopper for Long L10 1832
FDA UDI
ADIN DENTAL IMPLANT SYSTEMS LTD·07290105157270·
VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
PARADIGM SOF-SET ULTIMATE QR, MODELS 317 AND 318
FDA 510(k)
FDA Class 2
·General Hospital
Drill Stopper for Long L15/Short L10 1832
FDA UDI
ADIN DENTAL IMPLANT SYSTEMS LTD·07290105157300·
Widex
FDA UDI
Widex A/S·05706069721980·Widex D-FS BTE (Titan grey S-330 ) Telecoil, RC...
Widex
FDA UDI
Widex A/S·05706069720891·Widex UNIQUE U-PA BTE (Titan grey S-330 ) RC coil
Widex
FDA UDI
Widex A/S·05706069722406·Widex D-PA BTE (Titan grey S-330 ) RC coil
Widex
FDA UDI
Widex A/S·05706069722734·Widex CLEAR330 C3-FS BTE (Titan grey S-330 ) Te...
Widex
FDA UDI
Widex A/S·05706069721171·Widex BEYOND B-F2 (Titan grey S-330 ) Telecoil,...
Widex
FDA UDI
Widex A/S·05706069721669·Widex UNIQUE U-FS BTE (Titan grey S-330 ) Telec...
BD TRIAC CENTRIFUGE
FDA Adverse Event
Malfunction
·THE DRUCKER COMPANY·Product code GKG·May 1, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 10, 2011
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·August 6, 2008
COREVALVE TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·December 23, 2018
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code MMY·March 17, 2014
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code DXE·October 23, 2012