7 results
·
34ms
·
Sources: EU EUDAMED, US FDA
HOLLOW FIBER DIALYZER SERIES FOCUS 160/160H
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
STRIP, STERILIZATION INDICATOR; STEAM
FDA 510(k)
FDA Class 2
·General Hospital
KINETIC MODEL 330
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 25, 2014
SEE H-10
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code HQL·January 3, 2013
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·November 10, 2010
LOGIC CR TIB INSERT STD, SZ 2, 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 15, 2022