8 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CNAP Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
Vanguard Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304680647·
Vanguard Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304647886·
CALCIUM GEN. 2
FDA 510(k)
FDA Class 2
·Clinical Chemistry
RELIANCE SPINAL SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 18, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 29, 2011
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013