34 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS
FDA 510(k)
FDA Class 2
·Dental
MEDTRONIC PS MEDICAL CHANNELSCOPE ENDOSCOPE, MODELS 2232-001, 2232-002, 2232-003, 2232-004, 2233-002, 2233-005
FDA 510(k)
FDA Class 2
·Neurology
SOFT TISSUE SCREW AND WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
LINEAR 3-6
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 19, 2020
CAPSUREFIX NOVUS
FDA Adverse Event
Death
·MPRI·Product code DTB·April 23, 2013
EQUIPMENT DELIVERY SYSTEM , OSC-600
FDA Adverse Event
Malfunction
·STRYKER COMMUNICATIONS·Product code BRY·April 21, 2011
CAPSURE SP NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008
MAXPLUS POSITIVE PRESSURE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 30, 2021
MAXPLUS POSITIVE PRESSURE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 7, 2021
BD MAXPLUS¿ NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 16, 2021
MAXPLUS CLEAR NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·January 16, 2020
BD MAXPLUS¿ NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·October 26, 2022
MAXPLUS CLEAR NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·January 16, 2020
MAXPLUS POSITIVE PRESSURE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 10, 2021
MAXPLUS POSITIVE PRESSURE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 14, 2020
BD MAXPLUS¿ NEEDLELESS POSITIVE PRESSURE CONNECTOR
FDA Adverse Event
Malfunction
·Product code FPA·September 27, 2021
MAXPLUS POSITIVE PRESSURE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 30, 2021
CAPIOX FX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·May 22, 2025
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 5, 2022
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 16, 2022