9 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VYGON UMBILICAL CATHETHER INSERTION TRAY
FDA 510(k)
FDA Class 2
·General Hospital
LANDLEX, MODEL S403X
FDA 510(k)
FDA Class 2
·Physical Medicine
ACTION II Laser System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 7, 2018
RUSCH EQUIPLITE DISP METAL MAC 3
FDA Adverse Event
Malfunction
·TELEFLEX·Product code CCW·May 20, 2014
INTEPRO LARGE PORE POLYPROPYLENE MESH
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·February 12, 2013
ADULT BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·January 18, 2011
SCREW, FIXATION, BONE
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·March 8, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·March 11, 2016