10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ROSCH -THURMOND FALLOPIAN TUBE CATHETERIZATION SET
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
VERTEX® Reconstruction System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074239255·BONE SCREW 6955508 4.5 X 8MM CORTICAL
Zuma
FDA UDI
Seaspine Orthopedics Corporation·10889981097080·Zuma Implant/Trial Caddy 26mm x 24mm, 12 Deg
Duo Ti Expandable Interbody Fusion System
FDA UDI
SPINEOLOGY INC.·M7402955508·Duo Ti, 55 x 8mm, 0°
RUSCH SAFETY CLEAR PLUS CUFFED W/MAGILL TIP
FDA 510(k)
FDA Class 2
·Anesthesiology
DSL ACTIVE BETA2-MICROGLOBULIN (DSL 6500)
FDA 510(k)
FDA Class 2
·Immunology
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC INC.·Product code KWP·October 29, 2009
CARELINK
FDA Adverse Event
Malfunction
·RICE CREEK MFG·Product code DXY·February 11, 2013
TENDRIL ST
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011
MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT
FDA Adverse Event
C.T.M. SHANGHAI·Product code INI·July 24, 2014