13 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LIQUID FILLED RING TEETHER, MODEL 03807, LIQUID FILLED RING TEETHER, MODELS 1962005, 1962011, LIQUID FILLED TEETHING
FDA 510(k)
FDA Class 2
·Dental
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450309575·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450237854·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450806326·
SENICARE ADVANTIX POWDER FREE POLYURETHANE MEDICAL EXAMINATION GLOVE, SENSICARE ADVANTIX POWDER FREE POLYURETHANE DENTAL
FDA 510(k)
FDA Class 1
·General Hospital
DATASCOPE NITINOL CATHETER GUIDE WIRE (145 CM), DATASCOPE NITINOL CATHETER GUIDE WIRE (175 CM), DATASCOPE NITINOL CATHET
FDA 510(k)
FDA Class 2
·Cardiovascular
K09-10198 CONVENIENCE KIT
FDA Adverse Event
Injury
·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·April 30, 2009
K09-10198 CONVENIENCE KIT
FDA Adverse Event
Injury
·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·April 30, 2009
WAVEWRITER ALPHA? 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 12, 2026
PASSPORT 2 MONITOR
FDA Adverse Event
Malfunction
·MINDRAY DS USA, INC.·Product code DSI·April 30, 2013
BIOCOMPOSITE INTERFERENCE SCREW W/ DISP SHEATH
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MAI·September 16, 2014
STRETCHER CHAIR
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·April 20, 2011
UNKNOWN LIGASURE INSTRUMENT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·September 20, 2022