25 results
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30ms
·
Sources: EU EUDAMED, US FDA
PHILLIPS OMNIDIAGNOST ELEVA
FDA 510(k)
FDA Class 2
·Radiology
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR20320461·BioTorque wires Straight-Arch-F. max. .018"x.025"
SlimLine®
FDA UDI
ZIMMER SPINE, INC.·00889024403604·
ihcDirect® p120 Ab, 15mL
FDA UDI
NOVODIAX, INC.·00850000596900·Clone R1013
ihcDirect® p120 Ab, 5mL
FDA UDI
NOVODIAX, INC.·00850000596894·Clone R1013
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710410320460·Anterior Closing Wedge Osteotomy Guide, 32mm x ...
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710420320460·Anterio Lateral Wedge Osteotomy Guide, 32mm x 46mm
MODIFICATION TO AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100
FDA 510(k)
FDA Class 2
·Cardiovascular
VITAL SCIENTIFIC COAGULATION CONTROL,COAGULATION CONTROL LEVEL 1,2,3,QUIKCOAG COAGULATION CONTROL
FDA 510(k)
FDA Class 2
·Hematology
QUATTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 26, 2013
ACCU-CHEK ® INFORM METER
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·March 28, 2011
STERIS SYSTEM 1
FDA Adverse Event
Other
·STERIS CORPORATION·Product code MLR·April 21, 2008
SYNCHRO GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·April 8, 2010
SYNCHRO GUIDEWIRE
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·August 2, 2010
SYNCHRO GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·May 27, 2010
SYNCHRO GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·April 15, 2010
SYNCHRO-14 STRAIGHT 200-35CM
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code DQX·December 12, 2023
SYNCHRO-10 STRAIGHT 200CM
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code DQX·October 13, 2023
SYNCHRO-14 STRAIGHT 200-35CM
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code DQX·November 13, 2023
TITANIUM (TI) RIB SLEEVE-SIZE 8 220MM RADIUS
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code MDI·August 16, 2018