BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Medline ReNewal Reprocessed Harmonic FOCUS+ Shears without Adaptive Tissue Technology

    FDA 510(k)
    FDA Unclassified ·Unknown

    Scorpio

    FDA UDI
    Howmedica Osteonics Corp.·07613154020201·Posterior Stabilized Tibial Insert

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171029380·PESSARY, RING #0, W/SUPPORT, 1.75"

    EZ-IV MEDICAL PAD WARMING UNIT, MODEL 1000

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    POLYTEL(R) APT MODEL: PWA-08-01

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ORTHOPEDIATRICS BLADE PLATE SYSTEM

    FDA Adverse Event
    Injury ·ORTHOPEDIATRICS·Product code HRS·October 3, 2017

    RINGLOC-X E1 H/W 56/32MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·April 11, 2025

    BIODESIGN OTOLOGIC REPAIR GRAFT

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code KHJ·January 11, 2018

    UPHOLD VAGINAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 6, 2013

    IAB : 8 FR - 30 CC FOS

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·June 22, 2011

    CONSTRAINED ACETABULAR INSERTS

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code KWB·September 5, 2008