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

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    Clicky Cross

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526827882·***DISC*LEVAMED ANKLE SUPPORT BLACK VI

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613154648191·MINI PLATE,STRAIGHT,PROFILE HEIGHT 1.5MM

    NA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295086406·CANAL REAMER 13mm DIA

    CONNEX VITAL SIGNS MONITOR 6000 SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADVANTA SST GRAFT (>_6MM)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BAB FLEXIBLE FABRIC EXTRA LARGE

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC.·Product code KGX·June 16, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 5, 2025

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·March 31, 2026

    TARGETING ARM T2 PROX. HUM.

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA GMBH·Product code LXH·August 7, 2012

    ARCHITECT TOXO IGG

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·April 27, 2026

    ARCHITECT TOXO IGG

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·March 19, 2026

    MBT CEM KEEL TIB TRAY SZ3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·October 22, 2008

    QUATTRODE LEAD 3/4 MM, 30 CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 10, 2011

    CURRENT ACCEL VR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 8, 2013

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·April 8, 2026

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·March 4, 2026

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·April 2, 2026

    BD NEEDLE 21GA 2IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·November 9, 2021

    NEEDLE 21GA 2IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·September 20, 2021