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

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    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·Cross-Seal Suture-Mediated Vascular Closure Device System

    HERMES

    FDA UDI
    Smith & Nephew, Inc.·03596010493736·INTERFACE KIT HERMES TO S&N 400 INSUF

    EXPLOR

    FDA UDI
    Biomet Orthopedics, LLC·00880304210295·

    Anatomic Healing Cap 2mm

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118142874·Anatomic Healing Cap 2mm

    Multi-Unit H2mm

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118143147·Multi-Unit H2mm

    Anatomic Healing Cap 2mm

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011468·

    Multi-Unit H2mm

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011611·

    Bard Stinger Ablation Catheter: Item Numbers 210001 218501 L210001 210002 218502 L210002 210003 218503 L210003 210004 218504 L210004 210005 218505 L210005 210006 218506 L210006 210007 218507 L210007 210015 218516 L210008 210016 218518 L210009 210017 218519 L210010 210018 218520 L210011 210019 218521 L210012 210020 218523 L210013 210023 218524 L210014 210024 218525 L210015 210025 218526 L210016 210026 218527 L210017 210027 218528 L210018 210028 218529 210029 210030

    FDA Recall
    Terminated ·C. R.Bard, Inc./Electrophysiology Division·January 8, 2003

    TriplePlay

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377020902·FM1 - Alice 6

    STERILE PermaLoc Electrode, 60cm

    FDA UDI
    Synapse Biomedical, Inc.·00852184003144·

    Mariner

    FDA UDI
    Seaspine Orthopedics Corporation·10889981140724·Mariner Implant Tray, 10.5mm Iliac Caddy

    ACTOnco, ACTOnco IVD

    FDA 510(k)
    FDA Class 2 ·Pathology

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 5071 LEAD

    Full Field Digital, System, X-Ray, Mammographic

    FDA Pre-Market Approval
    FDA Class 2 ·SENOSCAN FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM

    Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BTS

    FDA Enforcement
    Class II ·Ongoing·Covidien, LP·April 10, 2024

    AMPLATZER SEPTAL OCCLUDER

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code MLV·February 20, 2024

    CARE ASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·June 27, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 12, 2011

    INCEPTA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 29, 2014

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·Myocardial Pacing Lead