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

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    Filters Regulation: Us FDA ×

    FRESENIUS ATR40 AND ATR120 AUTOTRANSFUSION RESERVOIRS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984586·anteriors; shade D2; mould Q 46

    DALE I.V. IDENTIFIER; PRODUCT #1125

    FDA 510(k)
    FDA Class 1 ·General Hospital

    COMFORTRON DENTAL ANESTHESIA APPARATUS

    FDA 510(k)
    FDA Unclassified ·Unknown

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    PROMOTE PLUS CRT-D, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·February 28, 2013

    ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NTE·February 11, 2011

    ACCU-CHEK ® AVIVA COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·August 6, 2014