BEUDAMED
    88 results · 23ms · Sources: EU EUDAMED, US FDA

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    SEGUIN ANNULOPLASTY RING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978959214·DISTRACTOR 9092310 STR HOUSING 10MM 4DEG

    Zavation

    FDA UDI
    Zavation LLC·00842166146457·eZspand PLIF/T-PLIF 9x23x10°, 10.5-15mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694044233·2.3mm x 10mm Mandible Safety Screw

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198574·AK3 Ultra Insert Trial Size 3, 10mm

    Titan Modular Shoulder System 2.5

    FDA UDI
    Smith & Nephew, Inc.·00885556859902·TSS GLENIOD INSTRUMENT TRAY - ...

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780243342·Titan™ Total Shoulder System The Titan Total Sh...

    CARDIOBEEPER CB12/12, MODEL CB12/12

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO:HL168D BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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·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

    UNKNOWN DEPUY SROM SLEEVE

    FDA Adverse Event
    Injury ·DEPUY (IRELAND) 9616671·Product code JDI·May 3, 2013