BEUDAMED
    73 results · 25ms · Sources: EU EUDAMED, US FDA

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    STANBIO BILIRUBIN TEST SET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Hader

    FDA UDI
    STERNGOLD DENTAL LLC·00841549115882·Hader Vertical Males Only, 6

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K1100550·Caddie, Misc Screws

    Momentum

    FDA UDI
    Ulrich Medical Usa, Inc.·00814386025843·Navigated tap, Ø 5.5mm, non-cannulated, 1/4"-sq...

    REVERSE MEDICAL REFLEX GUIDE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COOK VASCULAR ELECTROSURGICAL DISSECTION SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRISMATIC

    FDA Adverse Event
    Malfunction ·MAQUET S.A.S·Product code FTD·July 31, 2015

    PRISMATIC

    FDA Adverse Event
    Malfunction ·MAQUET S.A.S·Product code FTD·July 31, 2015

    PRISMATIC

    FDA Adverse Event
    Malfunction ·MAQUET S.A.S·Product code FTD·July 31, 2015

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·April 25, 2014

    PI1-3JUFXC

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code FZP·November 12, 2007

    MAXFIRE MARXMEN STRAIGHT

    FDA Adverse Event
    Injury ·BIOMET SPORTS MEDICINE·Product code MBI·October 31, 2012

    UNKNOWN MICROCATHETER

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code DQY·May 30, 2017

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 809A POTERIOR CHAMBER INTRAOCULAR LENS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 734A POSTERIOR CHAMBER INTRAOCULAR LENSES