8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPIFE ALKALINE HEMOGLOBIN
FDA 510(k)
FDA Class 2
·Hematology
RENASYS EZ
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NO. 86500 - ENDOSCOPIC JET WASHER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SMART PERFUSION PACK: APEX MBR FMC/MID WEST REG LEXINGTON, KY
FDA Adverse Event
Injury
·Product code DTZ·September 11, 2007
INRATIO2 PT/INR TEST STRIPS
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·March 17, 2016
AUTOPULSE NIMH BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC·Product code DRM·January 25, 2013
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·February 9, 2011
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 6, 2014