BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of entry for arthroscopic instruments into the joints.

    FDA Enforcement
    Class II ·Completed·Stryker Corporation·June 13, 2018

    Gambro ClinicalKit Safety Kit 15G, Catalog Number 0141080405C. Packaged 30 kits per case. Each kit contains 2 Nipro Safetouch Safety Needles.

    FDA Recall
    Completed ·Gambro Renal Products·November 13, 2002

    3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of entry for arthroscopic instruments into the joints.

    FDA Recall
    Completed ·Stryker Corporation·Product code PPR·December 21, 2017

    Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device

    FDA Recall
    Completed ·Boston Scientific Corporation·Product code LKK·May 11, 2026

    Invisalign Express 10 REF 8512 Invisalign System Comprehensive REF 9000 Invisalign System Moderate REF 9001

    FDA Recall
    Completed ·Align Technology Inc·Product code PNN·December 5, 2022

    MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display

    FDA Recall
    Completed ·Barco N.V. President Kennedypark 35 Kortrijk Belgium·Product code DXJ·April 24, 2024

    VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results VERIGENE System; invitro diagnostic test

    FDA Recall
    Completed ·Luminex Corporation·Product code PEN·April 16, 2025

    POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 6F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 8F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; NAUTILUS DELTA Tip Confirmation System (Includes: Netbook with Pre-loaded Software, Patient Module, and ECG Cable) Product Usage: Is an implantable access device designed to provide repeated access to the vascular system.

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·June 25, 2018