9 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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uPMR 790
FDA 510(k)
FDA Class 2
·Radiology
Oticon
FDA UDI
Sbo Hearing A/S·05714464034826·OTICON MORE 1 MINIBTE T C090 DEMO
MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate Fixation
FDA 510(k)
FDA Class 2
·Orthopedic
SkyOPS Orthopedic Plate System
FDA 510(k)
FDA Class 2
·Orthopedic
PACIFIC PLUS
FDA Adverse Event
Injury
·INVATEC TECHNOLOGY CENTER GMBH·Product code LIT·November 7, 2014
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 6, 2011
CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·July 18, 2013
BD ALARIS MEDICAL INFUSION SYSTEM ADMINISTRATION SETS
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·October 12, 2023
Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset Used in combination with infusion pumps for continuous subcutaneous infusion of medication.
FDA Enforcement
Class II
·Terminated·Unomedical As·July 1, 2015