7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANDREW LAPAROSCOPIC SURGICAL INSTRUMENTS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Malibu™
FDA UDI
Seaspine Orthopedics Corporation·10889981143480·Malibu Tray Lid
Meg-Ball Attachment System, Meg-Loc Abutment, Meg-Magnet Abutment
FDA 510(k)
FDA Class 2
·Dental
KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN
FDA 510(k)
FDA Class 2
·Cardiovascular
COBAS 6000 E601 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEW·December 2, 2010
2520274-2013-00282
FDA Adverse Event
Injury
·SYNTHES·Product code MJO·January 13, 2013
ENERGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 3, 2014