12 results
·
31ms
·
Sources: EU EUDAMED, US FDA
RADIOLOGICAL MARKING PEN
FDA 510(k)
FDA Class 1
·Radiology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192206·Apex Revision Knee Reamer – ZIMMER SHORT FLUTES...
ACUITY CENTRAL STATION, MODEL 020XXXXX (NOTE: XXXXX = VARIOUS CONFIG.)
FDA 510(k)
FDA Class 2
·Cardiovascular
Navik 3D
FDA 510(k)
FDA Class 2
·Cardiovascular
PK DISSECTING FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·June 5, 2014
EASYTRAK 2
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·October 4, 2010
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCO·Product code CBK·November 12, 2012
COMP LOCKING SCREW 4.75X35MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·February 15, 2019
VERSA-DIAL/COMPREHENSIVE TI STANDARD TAPER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·August 15, 2018
COMP RVRS SHDR GLEN BSPLT +HA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·February 15, 2019
COMP LOCKING SCREW 4.75X20MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·February 15, 2019
COMP LOCKING SCREW 4.75X15MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·August 15, 2018