BEUDAMED
    56 results · 27ms · Sources: EU EUDAMED, US FDA

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    Insight BD

    FDA 510(k)
    FDA Class 2 ·Radiology

    ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EYE CARE CURE CONTACT LENS CASE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 30, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 5, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 13, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 14, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 18, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 8, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 30, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 31, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 6, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 14, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 30, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 1, 2026

    UNKNOWN DEPUY ACETABULAR SCREW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HWC·October 15, 2014

    DPM 7

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code MHX·May 21, 2013