7 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACUFEX MENISCAL RASPS
FDA 510(k)
FDA Class 2
·Orthopedic
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668103081·KATENA FEMTO SPATULA, DOUBLE ENDED
PROFILE BBL SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Disposable electrosurgical pencil (MD1000)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HUDSON SHERIDAN/HVT TRACHEAL TUBE
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTR·January 24, 2013
PUMP,COLLEAGUE SINGLE CHANNELCOLOUR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 17, 2010
ENDOWRIST ONE VESSEL SEALER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·July 14, 2014