8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KSEA URETERO-RENO-FIBERSCOPE AND NEPHRO-FIBERSCOPE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
artegral
FDA UDI
Merz Dental GmbH·D7091970427·anteriors; shade D3; mould UCS
DUPEL TRANSPORT IONTOPHORESIS SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
Anprolene SteriTest
FDA 510(k)
FDA Class 2
·General Hospital
E-CAM COINCIDENCE MODE [510 (K) K970627)
FDA Adverse Event
Malfunction
·SIEMENS MEDICAL SYSTEMS, INC., NMG GROUP·Product code IYX·April 20, 2001
FENESTRATED BIPOLAR FORCEPS INSTRUMENT
FDA Adverse Event
Injury
·INTUITIVE SURGICAL,INC.·Product code NAY·February 20, 2013
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·January 18, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 31, 2014