7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
LASERFLO(R) BLOOD PERFUSION MONITOR (MODEL BPM2)
FDA 510(k)
FDA Class 2
·Cardiovascular
OMNIDOS
FDA 510(k)
FDA Class 2
·Radiology
PATHASSIST LIGHT FIBER
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021
GORE TAG THORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES,INC·Product code MIH·November 23, 2010
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code LWS·January 11, 2013
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code LWS·July 3, 2014