12 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DENVER PLEURX PLEURAL CATHETER KIT, CATALOG NO. 50-7000, DENVER PLEURX HOME DRAINAGE KIT, CATALOG NO. 50-7500
FDA 510(k)
FDA Class 2
·Cardiovascular
PLEURX DRAINAGE KIT 500ML 10/CS
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code DWM·July 25, 2025
PLEURX DRAINAGE KIT 500ML 10/CS
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code DWM·December 24, 2024
PLEURX DRAINAGE KIT 500ML 10/CS
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code DWM·December 24, 2024
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704294088·
NA
FDA UDI
KEY SURGICAL, INC.·10849771050152·Steinmann Pins, Double trocar threaded, 3/32-in...
Key Surgical K-Wires and Steinmann Pins
FDA UDI
KEY SURGICAL, INC.·00849771015505·Steinmann Pins, Double trocar threaded, 3/32-in...
MASTERSCREEN PNEUMO & MASTERSCOPE
FDA 510(k)
FDA Class 2
·Anesthesiology
BOND Ready-to-Use (RTU) Primary Antibody Progesterone Receptor (16), Novocastra Liquid Mouse Monoclonal Antibody Progesterone Receptor Clone 16
FDA 510(k)
FDA Class 2
·Hematology
PENTA
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 30, 2013
STEDY
FDA Adverse Event
Malfunction
·BHM MEDICAL, INC.·Product code FSA·January 12, 2011
TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 31, 2014