29 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SILVERSPEED HYDROPHILIC GUIDEWIRE, X-CELERATOR HYDROPHILIC EXCHANGE GUIDEWIRE, X-PEDION HYDROPHILIC GUIDEWIRE, MIRAGE HY
FDA 510(k)
FDA Class 2
·Cardiovascular
MALLORY HEAD HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304225121·
Arthrex®
FDA UDI
ARTHREX, INC.·00888867005976·BONE PLUG IMPACTOR, 7MM
SUNDER CENTRAL VENOUS CATHETER KIT, MODELS SD-3L55F30J AND SD-3L70F30J
FDA 510(k)
FDA Class 2
·General Hospital
2MP MONOCHROME LCD MONITOR, RADIFORCE GX240
FDA 510(k)
FDA Class 2
·Radiology
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237315·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237254·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237285·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237292·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237261·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237247·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237278·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237308·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971352·
Ascend
FDA UDI
ALPHATEC SPINE, INC.·00190376668659·12mm CORE, NANOTEC BAN 12 x 40 mm 7°
Ascend
FDA UDI
ALPHATEC SPINE, INC.·00190376669274·12mm CORE, NANOTEC KBN 12 x 40 mm 7°
PERSONA PS STANDARD FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·September 18, 2018
PERSONA STEMMED TIBIAL CEMENTED
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·September 18, 2018
EMAX 2 PLUS MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·May 22, 2013
TRANSVENE SVC/CS
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code LWS·June 14, 2011