8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SmartTouch
FDA 510(k)
FDA Class 2
·Anesthesiology
CRYONIZE TM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL
FDA 510(k)
FDA Class 2
·Radiology
MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 36 SIZE M
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·April 27, 2018
3.0MM TI STERNAL LCKNG SCREW SELF-DRILLING/20MM
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·June 17, 2013
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·July 23, 2011
COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 25, 2008
TENSION FREE VAGINAL TAPE - EXACT UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·June 3, 2021