7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756683470·LAPAROTOMY PACK
CANDELA UPC LASER PHOTOCOAGULATOR
FDA 510(k)
FDA Class 2
·Ophthalmic
PATIENT EXAMINATION GLOVES (LATEX)
FDA 510(k)
FDA Class 1
·General Hospital
HS III PROXIMAL SEAL SYTEM 3.8MM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code DXC·December 28, 2012
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 16, 2014
TENDRIL STS
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010