44 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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COULTER ACT 5DIFF AL HEMATOLOGY ANALYZER
FDA 510(k)
FDA Class 2
·Hematology
Medial Pilon Plate, Right, Short, 13-Hole
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665024661·
Battalion
FDA UDI
ALPHATEC SPINE, INC.·00840967187488·Battalion, LLIF Trial, 15°, 20 mm Wide, 13 mm X...
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0120130·Screwdriver, Polyaxial, Standard, Fixed Tap Sle...
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710620320130·Quad Channel Met-Traverse, 32mm x 13mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710810320130·Dwyer Calcaneal Guide, 32mm x 13mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710820320130·Zadik Calcaneal Guide, 32mm x 13°
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710450320130·Medial Guide, Closing Wedge Osteotomy, 32mm x 13mm
OMNIPORT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LIFESOURCE MODELS UA-787, UA 787PC, UA-787T
FDA 510(k)
FDA Class 2
·Cardiovascular
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 20, 2019
SCP PANEL CENTRIFUGE JMS
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DWA·November 5, 2013
SCP PANEL CENTRIFUGE JMS
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DWA·March 14, 2014
SCP CONTROL PANEL
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012
CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DWA·January 19, 2018
CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND GMBH·Product code DWA·January 5, 2022
STOCKERT JMS CENTRIFUGAL PUMP SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 26, 2013
COLLEAGUE TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 28, 2011
ORTHO PROVUE
FDA Adverse Event
Malfunction
·MICRO TYPING SYSTEMS, INC.·Product code KSZ·April 21, 2008