7 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COVIDIEN WARMTOUCH CONVECTIVE WARMING UNIT
FDA 510(k)
FDA Class 2
·Cardiovascular
AGILIS ES STEERABLE INTRODUCER
FDA 510(k)
FDA Class 2
·Cardiovascular
SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800
FDA 510(k)
FDA Class 2
·General Hospital
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
CONSMA·Product code ITJ·May 21, 2013
EXCELON TRANSBRONCHIAL ASPIRATION NEEDLE, MODELS 6410, 6411, 6412
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code EOQ·June 14, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 20, 2008
NOVOSYN VIOLET7/0(0.5)45CM2XDLM6S200M
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAM·January 9, 2024