8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
FLEXTIP GRASPER
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
PRESTIGE LP™
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994493712·DISC 6972450 PRESTIGE
ESPRIT VENTILATOR AUTO-TRAK SENSITIVITY OPTION, MODEL V1000
FDA 510(k)
FDA Class 2
·Anesthesiology
TENS device-HeadaTerm, eEspress
FDA 510(k)
FDA Class 2
·Neurology
MICRODEBRIDER 1898200T IGS M4
FDA Adverse Event
Malfunction
·XOMED MFG JACKSONVILLE·Product code ERL·February 21, 2013
ADAPTER SLEEVES 12/14 +5
FDA Adverse Event
Injury
·DEPUY INTL., LTD.·Product code KWA·January 26, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·August 1, 2014
PECTUS SYSTEM JANTON 12" TI PECTUS BAR 3.048CM (12") (L) TITANIUM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·January 2, 2019