BEUDAMED
    7 results · 53ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    IV KIT 100 CS

    FDA Adverse Event
    Injury ·MEDICAL ACTION INDUSTRIES·Product code LRS·January 6, 2026

    IV KIT 100 CS

    FDA Adverse Event
    Injury ·MEDICAL ACTION INDUSTRIES·Product code LRS·January 6, 2026

    5MM ELASTIC STAYS 8/PK

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GAD·April 11, 2018

    Mobi-C 14mm Distraction Screw, Quick Start. Intended for cervical intervertebral disc replacement. Item Number: 0024-LDR TEDAN SURGICAL INNOVATIONS LLC DISTRIBUTED BY: LDR SPINE USA, INC., 13785 RESEARCH BLVD, SUITE 200- AUSTIN, TX 78750 Product Usage: The device is intended as a cervical intervertebral disc replacement at one or two contiguous levels from C3 to C7 designed to maintain/restore segmental motion and disc height. MOBI-C distraction pins are inserted into the vertebral body below and above the disc that is to have the disc replacement. The pins are then attached to a locking retractor/distractor to open up the disc space in order to complete the discectomy and overall distraction during the surgery

    FDA Recall
    Terminated ·Zimmer Biomet, Inc.·Product code LXH·April 1, 2019

    CEpartner4U

    Authorized representative
    🇳🇱 Netherlands·160 Manufacturers·5787 Devices

    MedPath GmbH

    Authorized representative
    🇩🇪 Germany·537 Manufacturers·13464 Devices

    SUNGO Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·1571 Manufacturers·20390 Devices