BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    SLIDING BOARD

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Bard® Urethral Catheterization Tray with Vinyl Catheter

    FDA UDI
    C. R. Bard, Inc.·00801741030437·Bard® Urethral Catheterization Tray with Vinyl ...

    BARD® URETHRAL CATHETERIZATION TRAY WITH RED RUBBER CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·May 9, 2022

    SILC® Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMITH & NEPHEW MIS HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BARD® URETHRAL CATHETERIZATION TRAY WITH VINYL CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·May 9, 2022

    BARD® URETHRAL CATHETERIZATION TRAY WITH VINYL CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·October 31, 2018

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    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·August 28, 2012

    ACRYSOF

    FDA Adverse Event
    Malfunction ·ALCON MANUFACTURING, LTD.·Product code HQL·December 18, 2013

    BASIS SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·July 23, 2010

    LCP PROX-FEMPL 4.5/5 LE SHAFT 4HO L175 S

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code HRS·June 25, 2013

    Current, Sterile EO, Model #/ Part #: 1207-30/50020236-001, 60010739-207, 60010739-407; 1207-36/50020237-001, 60010742-207, 60010742-307, 60010742-407, 60010742-707; 2207-30/ 50020238-001, 60010738-207; 2207-36/ 50020239-001, 60010741-207, 60010741-307, 60010741-407, 60010741-707; CD1211-36/100006983, 100012542, 100016679, 100031495, 100035634, 100035635, 100042587, 100047090; CD1211-36Q/100004079, 100004081, 100019783, 100035607, 100042591, 100047191; CD1215-36/100006990, 100010230, 100010241, 100010242, 100010244, 100012563, 100012564, 100034631, 100046574, 100046786; CD1215-36Q/100006768, 100006769, 100006770, 100023300, 100030306, 100033794, 100042402, 100046720, 100046904; CD1217-36/100011824; CD1219-36/100002160, 100002864, 100011826; CD1219-36Q/100004071, 100023301; CD2211-36/100006982, 100012536, 100016678, 100031440, 100035629, 100035636, 100042520, 100047192; CD2211-36Q/100004085, 100004087, 100019782, 100035587, 100042575, 100047193; CD2215-36/100006992, 100010224, 100010226, 100010227, 100010228, 100012515, 100012516, 100036606, 100046676, 100046792, 60019063; CD2215-36Q/100006762, 100006763, 100006764, 100023302, 100029180, 100033793, 100042404, 100046789, 100046905; CD2217-36/100011828, 100046991, 60016124-401; CD2219-36/100002139, 100002140, 100002862, 100011830; CD2219-36Q/100023303

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018