8 results
·
17ms
·
Sources: EU EUDAMED, US FDA
BONE & MARROW CLLECTION SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902974489·INSTRUMENT 6971268 IMP TRIAL 8X16MM
MICROSCAN SYNERGIES PLUS GRAM POSITIVE MIC/COMBO PANELS WITH TETRACYCLINE
FDA 510(k)
FDA Class 2
·Microbiology
Reverse 021 Micro Catheter, Reverse 027 Micro Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
DHS/DCS-SCR Ø12.5 L100 SST
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code KTT·February 21, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·January 26, 2011
SOLETRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 31, 2014
REMINGTON MEDICAL DISPOSABLE PACING CABLE
FDA Adverse Event
Malfunction
·REMINGTON MEDICAL·Product code DSA·September 13, 2002