7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Beta-2-Microglobulin
FDA 510(k)
FDA Class 2
·Immunology
VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM MODEL 50020
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ANSPACH IMRI SAFE SURGICAL DRILL SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
DRILL BIT Ø3.2 CALIBR L474 3FLUTE F/HIPS
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HTW·June 11, 2013
PATCH
FDA Adverse Event
Injury
·HISTORICAL CPI ST. PAUL·Product code NHW·July 13, 2011
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code NIQ·September 15, 2008
cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V
FDA Enforcement
Class II
·Terminated·Roche Diagnostics Corporation·March 14, 2018