BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    ARC-EX System

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Novo Surgical Inc.

    FDA UDI
    NOVO SURGICAL, INC.·00842331136665·shortbent stitch scissors, curved, delicate pat...

    ER-REBOA Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INION S-1 BIODEGRADABLE ANTERIOR CERVICAL FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·October 28, 2021

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·November 14, 2014

    CODMAN* LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF - RAYNHAM·Product code JXG·September 16, 2011

    URETEX SUPPORT PP TRANSOBTUR2 KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·July 18, 2013

    BE POD®

    FDA UDI
    FOURNITURES HOSPITALIERES INDUSTRIE·03661489518218·

    DEKA MOTUS AZ

    FDA Adverse Event
    Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·March 8, 2024

    AXIUM PRIME BRPL HLX

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·March 20, 2022