28 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BWIII EEG, BWIII EEG PLUS, BWIII PSG, BWIII PSG PLUS
FDA 510(k)
FDA Class 2
·Neurology
FAC-4 - Miller & Long Concrete
FDA UDI
Certified Safety Manufacturing, Inc.·00766588121079·FAC-4 - Miller & Long Concrete
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08806390849593·
CLEARFIX RIGID STERNAL FIXATION Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089436866·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08806390849609·
Kroger
FDA UDI
KROGER CO., THE·00041260345203·KROGER INSTANT EAR THERMOMETER
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089479429·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089479436·
LIVESURE PHENECYCLINE (PCP) SCREEN TESTS
FDA 510(k)
FDA Unclassified
·Unknown
OSSTAPLE CHILL
FDA 510(k)
FDA Class 2
·Orthopedic
CLEARFIX RIGID STERNAL FIXATION Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089446650·
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·May 19, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·January 16, 2023
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 7, 2022
ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-RIO
FDA Adverse Event
Malfunction
·MAKO SURGICAL·Product code OLO·April 25, 2014
BD VACUTAINER® PLUS PLASTIC WHOLE BLOOD TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·November 3, 2017
ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-RIO
FDA Adverse Event
Malfunction
·MAKO SURGICAL·Product code NPJ·April 25, 2014
LAMITRODE TRIPOLE 16C LEAD, 60 CM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 29, 2015
QUANTUM SYSTEM
FDA Adverse Event
Malfunction
·ARTHROCARE CORPORATION·Product code GEI·May 7, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 23, 2014