10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STERILE LEMAITRE GLOW 'N TELL TAPE
FDA 510(k)
FDA Class 2
·Physical Medicine
ACESSA GUIDANCE HANDPIECE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SIMPLISCRIPTOR EK 31/101 037 16
FDA 510(k)
FDA Class 2
·Cardiovascular
COREVALVE SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CORONARY AND STRUCTURAL HEART·Product code NPT·June 6, 2017
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·April 13, 2020
UNSPECIFIED SAFESET TRANSPAC SETS
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025
NEXGEN GSF LPS-FLEX FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·January 25, 2013
UNKNOWN ZIMMER KNEE
FDA Adverse Event
Malfunction
·ZIMMER, INC.·Product code JWH·December 14, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 14, 2014
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·December 7, 2017