8 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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POLYSORB SUTURE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYNCHRON CREATINE KINASE REAGENT
FDA Adverse Event
BECKMAN COULTER INC.·Product code CGS·June 17, 2011
Endoform Reconstructive Template - Non Absorbable
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STEREOTACTIC HEAD AND NECK LOCALIZER, MODEL 50-100
FDA 510(k)
FDA Class 2
·Radiology
ENDOPATH ENDOSCOPIC MULTIFEED STAPLER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GAG·April 6, 1998
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 28, 2013
UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code LGD·February 8, 2011
DELTAPAQ - CERECYTE MICROCOIL
FDA Adverse Event
Malfunction
·MICRUS ENDOVASCULAR, LLC·Product code HCG·August 5, 2014