7 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Swoop Portable MR Imaging System
FDA 510(k)
FDA Class 2
·Radiology
PRECISET DAT PLUS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SMITH & NEPHEW, INC. TOTAL KNEE SYSTEM INSTRUMENTATION
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 13, 2025
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 3, 2014
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS NEUROVASCULAR, INC.·Product code NJE·August 24, 2011
2.7MM 30° AUTOCLAVABLE STUBBY ARTHROSCOPE W/ SPEEDLOCK
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY-SAN JOSE·Product code HRX·July 11, 2013