BEUDAMED
    13 results · 28ms · Sources: EU EUDAMED, US FDA

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    QM300 CALIBRATOR G PACK

    FDA 510(k)
    FDA Class 1 ·Microbiology

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909108852·REVELATION DIAMOND 863-016C - 5 PACK

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756379687·PV PACK

    BD CD81 APC-H7 (JS-81) ASR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code MVU·July 14, 2020

    Elevation Spine Saber-C System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNI-LASER 470

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SYNCHRON (R) SYSTEMS CREATININE REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code CGX·July 2, 2011

    PROULTRA ENDO TIPS

    FDA Adverse Event
    Malfunction ·DENTSPLY MAILLEFER·Product code ELC·June 8, 2006

    DURASTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·November 23, 2010

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 11, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code FSA·July 2, 2014

    SMITHS MEDICAL PORTEX TRACHEOSTOMY TUBE BLUE LINE ULTRA

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code JOH·November 18, 2019

    PORTEX BLUE LINA ULTRA SUCTIONAID TRACH TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·July 5, 2022