35 results
·
27ms
·
Sources: EU EUDAMED, US FDA
MEGABEAM SIDEFIBER FIBER OPTIC DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Molift
FDA UDI
Etac A/S·05707995001832·
Humelock Reversed Shoulder
FDA UDI
FX SOLUTIONS·03701037321140·STARTER Ø06mm / HUDSON
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 50mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665020755·
Molift
FDA UDI
Etac A/S·05707995001849·
Canaveral®
FDA UDI
FLOSPINE LLC·B183120600500·6.0mm Curved Rod, Ti Alloy 50mm
Persona® PPS®
FDA UDI
Zimmer, Inc.·00889024631427·
Persona® PPS®
FDA UDI
Zimmer, Inc.·00889024631410·
TOP QUALITY CHLORINATED-POWDERFREE EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ADVIA CENTAUR AND ACS: 180 FOLATE IMMUNOASSAY
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SELOX JT 53
FDA Adverse Event
Other
·BIOTRONIK GMBH AND CO·Product code DTB·June 29, 2006
S5 CONTROL DISPLAY MODULE
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·August 8, 2012
S5 DOUBLE HEAD PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
S5 DOUBLE HEAD PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
SEE H10
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013
S5 DOUBLE HEAD PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·August 29, 2012
S5 CONTROL DISPLAY MODULE
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 16, 2012
S5 CONTROL PANEL
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 15, 2012
S5 CONTROL DISPLAY MODULE
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 16, 2012
AED PLUS
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·March 19, 2013