BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound Systems

    FDA 510(k)
    FDA Class 2 ·Radiology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704920706·

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704266627·FRAZIER SUCTION TUBES 7.5" ANGLED 11 FRENCH

    CUFFLINK(TM) KNOTLESS ANCHOR WITH INSERTER, 4.5MM/5.5MM - PEEK ONLY, CUFFLINK SP(TM) KNOTLESS ANCHOR WITH INSERTER, 4.5

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    URS LP DIGITAL, MILLENNIUM, RADPRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    INDIGO SYSTEM ASPIRATION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code QEW·August 7, 2023

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·June 3, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 30, 2014

    ENDOPATH STEALTH CIR STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code KOG·June 28, 2011

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·February 22, 2019

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·September 5, 2017