BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    STERI-PAK BOWIE DICK TEST PACK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Modulus

    FDA UDI
    Nuvasive, Inc.·00195377049988·Modulus ALIF Trial, 12x42x32mm 15°Lrg

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982188·posteriors; shade D2 light; size M; upper jaw

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123847·K-WIRE - DOUBLE TROCAR 1.8mm DIA x 200mm

    Ion Endoluminal System ; Flexision Biopsy Needle

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    TYMPANOSTOMY TUBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·January 18, 2011

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 5, 2014

    CALSTRUX (TRICALCIUM PHOSPHATE)

    FDA Adverse Event
    Injury ·STRYKER BIOTECH·Product code MPY·December 15, 2006