292 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Sclerotherapy & Endoscopic Needles
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693263177·The blades and knifes consumables are for use w...
SMARTSCREW MODEL 222006...227510
FDA 510(k)
FDA Class 2
·Orthopedic
Altus Spine Interbody Fusion System
FDA UDI
Altus Spine, LLC·00843210131559·Broach Trial
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690127888·Adjustable Modular Tibia Tray Trial Size 6
G-SCAN BRIO
FDA 510(k)
FDA Class 2
·Radiology
CONDUCTIVE GEL
FDA 510(k)
FDA Class 2
·Neurology
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243118·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243187·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243156·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243149·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243132·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243170·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243163·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243125·
COAGUCHEK S SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JPA·August 21, 2006
EPIDURAL CATHETER
FDA Adverse Event
Injury
·ARROW INTERNATIONAL, INC.·Product code BSO·March 22, 2006
ZIMMER PERIARTICULAR LOCKING PLATE SYSTEM LOCKING SCREW
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code HWC·June 2, 2006
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·January 5, 2007
LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code FZP·June 22, 2006