BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    PERFUSION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ER-REBOA Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CONFLUENT SURGICAL EXTENDED TIP APPLICATOR, MODEL 70-2008-008

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MONOCRYL PLUS SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·June 13, 2014

    IN TOUCH ZU

    FDA Adverse Event
    STRYKER MEDICAL QUEBEC LP·Product code FNL·October 8, 2010

    OMNILINK ELITE PERIPHERAL STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIO·December 13, 2012

    Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633 Product Usage: Partial Shoulder Replacement.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019