11 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARVIS® Shoulder
FDA 510(k)
FDA Class 2
·Neurology
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613018009·K-Wire, Single Ended, Trocar Point, Diameter Si...
Audilab
FDA UDI
Sbo Hearing A/S·05714464052554·ALIGO 1 FW 1.3.0
FSC ANTI-STATIC VALVED COLLAPSIBLE HOLDING CHAMBER
FDA 510(k)
FDA Class 2
·Anesthesiology
LEVIA PHOTOTHERAPY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Trilogy®
FDA UDI
Zimmer, Inc.·00889024119390·
CORB®
FDA UDI
Zimmer, Inc.·00889024066298·
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON ¿ IRVINE TECHNOLOGY CENTER·Product code HQC·November 4, 2014
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·July 11, 2013
WATCHMAN LAA CLOSURE DEVICE & DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NGV·December 17, 2024