12 results
·
17ms
·
Sources: EU EUDAMED, US FDA
MODEL ALPHA TS-2
FDA 510(k)
FDA Class 1
·Radiology
Barco
FDA UDI
FIMI SRL·05415334002272·MDRC-2321 STIB
BIO-GUARD O.R. SCRUB PREP TRAY
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ALLKARE BARRIER WIPE
FDA 510(k)
FDA Class 1
·General Hospital
BIOLOX DELTA CERAMIC TAPER LINER, SIZE GG / 32 I.D.
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·July 1, 2019
NA
FDA UDI
Zimmer, Inc.·00889024077607·
NA
FDA UDI
Zimmer, Inc.·00889024077584·
NA
FDA UDI
Zimmer, Inc.·00889024077591·
ANCHOR C DIAM.3.5MM SELF DRILLING 10MM
FDA Adverse Event
Malfunction
·STRYKER SPINE-FRANCE·Product code OVE·January 30, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·December 21, 2010
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·July 15, 2014
BIOLOX DELTA, CERAMIC FEMORAL HEAD, S,¸ 32/-3.5, TAPER 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·July 1, 2019