8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
GEN. DIAG. CHROMOSTRATE REF. PLASMA
FDA 510(k)
FDA Class 2
·Hematology
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209110377·
Shoreline™ ACS
FDA UDI
Seaspine Orthopedics Corporation·00889981142332·No Profile Spacer, 20x15x9mm, 7 Degree, Sterile
Disposable Balloon Catheter (B5-2Q); Disposable Balloon Catheter (B7-2Q); Disposable Balloon Catheter (B7-2LA)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
VIVACE Electrosurgical System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 30, 2014
SYMBIQ SINGLE CHANNE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·November 26, 2012
ADVANCE 2000 W/SCALE
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·September 20, 2010