31 results
·
22ms
·
Sources: EU EUDAMED, US FDA
SPARC SLING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00112511·
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040015308·Zirlux 16+ C4 85x40x22
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254172·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254158·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254134·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254141·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254165·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254103·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254127·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254189·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254097·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254196·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254110·
SNIPER, MODEL OR-3872XX SERIES
FDA 510(k)
FDA Class 2
·Cardiovascular
EVIS EXERA GASTROINTESTINAL VIDEOSCOPE GIF-Q160Z
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EMBOSHIELD NAV6 EMBOLIC PROTECTION SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NTE·March 12, 2010
ACCESS 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·November 15, 2011
SOFTCLIX ® LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·March 19, 2013
MINI-CAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·March 8, 2011