8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
MODIFIED LYOFOAM WOUND DRESSINGS
FDA 510(k)
FDA Class 1
·General Hospital
LABEL, STERILIZATION INDICATOR; RADIATION
FDA 510(k)
FDA Class 2
·General Hospital
FC-101 FEMORAL CATHETER GUIDE WIRE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
STEAM STER LOCKS ORANGE
FDA Adverse Event
Injury
·AESCULAP INC·Product code KCT·October 12, 2016
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 25, 2014
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
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·January 3, 2013
STEAM STER LOCKS ORANGE
FDA Adverse Event
Malfunction
·AESCULAP INC·Product code KCT·July 26, 2016