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

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    SYNGO CIRCULATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809847833·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE EXTRA LA...

    CONMED

    FDA UDI
    Conmed Corporation·10845854023389·EXTENSION HOSE WITH DISS/SCHRADER CONNECTOR, 10'

    REMEDY MODEL 2Z12

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ZOLL M SERIES NIBP OPTION, MODEL MSERIES NIBP OPTION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GMK 3D METAL TIBIAL TRAY

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 11, 2025

    OUTRIGGER TARGETING GUIDE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 8, 2021

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 16, 2025

    Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2424902B 09/05/2029

    FDA Enforcement
    Class II ·Ongoing·O&M HALYARD INC·September 10, 2025

    ASR ACETABULAR IMPLANT 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·April 11, 2013

    VISTA BRITE TIP GUIDING CATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DQY·May 20, 2008

    EASYTRAK 3

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·April 12, 2011

    PEN NDL 32G 4MM PRO 100 BOX FR

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·December 26, 2024

    DOUBLE MOBILITY LINER

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·June 6, 2025

    PEN NDL 32G 4MM PRO 100 BOX FR

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·December 26, 2024

    SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·April 4, 2025

    Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2424902B 09/05/2029

    FDA Recall
    Open, Classified ·O & M HALYARD INC·Product code KKX·July 17, 2025

    DOUBLE MOBILITY LINER

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·April 11, 2025

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·September 16, 2020

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·March 27, 2020