BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    BACT/ALERT PEDI-BACT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110966·STERILIZING CASE 4-KNIVES

    DELTA PROTR.LINER ØINT 36MM #L

    FDA Adverse Event
    Malfunction ·LIMACORPORATE S.P.A.·Product code LPH·January 3, 2020

    TROJAN MAGNUM CONDOM WITH WARMING LUBRICANT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MICROSCAN PLUS GRAM NEGATIVE MIC/COMBO PANELS WITH MEROPENEM (0.12-32 UG/ML)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    TROJAN PLEASURE PACK LUBRICATED CONDOMS

    FDA Adverse Event
    Injury ·CHURCH & DWIGHT CO., INC.·Product code HIS·October 29, 2014

    ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 19, 2016

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 1, 2016

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·December 10, 2010

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·January 17, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 8, 2014