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

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    MONTAGE Settable, Resorbable Bone Putty

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bernafon

    FDA UDI
    Bernafon AG·05714464008940·BERNAFON ALPHA 9 MNR T R ANBR

    Class B 21 Retrofit - ZLB

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588220635·Class B 21 Retrofit - ZLB

    SAFEPRO SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTELLISAVE AX700 ANESTHESIA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·November 3, 2008

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 24, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·July 1, 2013

    BD KIESTRA IDENTIFA

    FDA Adverse Event
    Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·October 8, 2025

    BD KIESTRA¿ IDENTIFA

    FDA Adverse Event
    Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·December 9, 2024

    HEARTMATE®, 14V LI-ION RECHARGEABLE BATTERY SET

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·January 29, 2025