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

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    STOPSBLEEDING TOPICAL HEMOSTAT POWDER AND FOAM

    FDA 510(k)
    FDA Unclassified ·Unknown

    ALLIS TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896023567·ALLIS TISSUE FORCEPS BABY TIP

    HYDROFIX SURGICAL SHEET

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

    HRV TOOLS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 16, 2023

    BD INTIMA-II CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·January 13, 2021

    BD INTIMA-II CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·January 13, 2021

    BD INTIMA-II CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·December 9, 2020

    INOMAX DSIR (DELIVERY SYSTEM)

    FDA Adverse Event
    Injury ·MALLINCKRODT MANUFACTURING LLC.·Product code MRN·January 10, 2021

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 15, 2011

    ZEPHYR XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 13, 2014

    V40 COCR LFIT HEAD 36MM/0

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·May 31, 2013

    ProScreen 6 Panel Cup w/Adult (AU), Item No. PSCupA-6MBAU

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015