8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PAB IV CONTAINER
FDA 510(k)
FDA Class 2
·General Hospital
OMNI Knee
FDA UDI
Omni Life Science, Inc.·00841690101994·All Poly 3 Peg Patella 38 mm x 8 mm
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690110750·Patella Trial 38mm x 8mm
NEXT GENERATION SALEM SUMP
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LUMENIS PULSE 120H
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·May 30, 2014
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 20, 2012
PATIENT ROOM WALL SAVER RECL
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIV.·Product code FRK·September 10, 2010