7 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SHILEY FENESTRATED REUSABLE INNER CANNULA, MODIF
FDA 510(k)
FDA Class 2
·Anesthesiology
ASEPTICO ENDOPEX V, MODEL AEU-40
FDA 510(k)
FDA Unclassified
·Unknown
REUNION RSA SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HU-FRIEDY PERMA SHARP SUTURES
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code GAR·May 26, 2010
OT LANCETS
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 16, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 28, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·July 12, 2014