BEUDAMED
    357 results · 27ms · Sources: EU EUDAMED, US FDA

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    A & D MEDICAL LIFESOURCE UA-704 DIGITAL BLOOD PRESSURE MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Baltic Denture System BD Load

    FDA UDI
    Merz Dental GmbH·D7091032499·Baltic Denture System BDLoad ↓ Mn7 PLSEum2DFm C...

    ACE SurgicalCh Gut 5-0 14" T28

    FDA UDI
    Surgical Specialties México, S. de R.L. de C.V.·00848782022915·003-2499 Ch Gut 5-0 14" T28

    BRENTWOOD IQMARK DIGITAL SPIROMETER (INCLUDES DISPOSABLE PNEUMOTACH MOUTHPIECES AND 3-LITER CALIBRATION SYRINGE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ENVIRON-NP POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TELEPORT

    FDA Adverse Event
    Malfunction ·INTERVENTIONAL SPINE, INC.·Product code FZX·February 28, 2011

    ACRYSOF TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·April 1, 2013

    SYNERGY

    FDA Adverse Event
    Injury ·MEDTRONIC EUROPE SARL·Product code LGW·March 24, 2011

    HEPARIN I.V. FLUSH SYRINGE 100 UNITS/ML

    FDA Adverse Event
    Other ·MEDEFIL, INC.·Product code NZW·April 21, 2008

    PERPOS PLS SYSTEM

    FDA Adverse Event
    Malfunction ·INTERVENTIONAL SPINE, INC.·Product code MRW·February 28, 2011

    PERPOS PLS SYSTEM

    FDA Adverse Event
    Malfunction ·INTERVENTIONAL SPINE, INC.·Product code MRW·February 28, 2011

    Toshiba Excelart VANTAGE Model MRT-1503, Magnetic Resonance Imaging Systems, Regulation Number 21 CPR 892.1000, Regulatory Class II, Product Code 90-LNH and was cleared with K032490

    FDA Recall
    Terminated ·Toshiba American Med Sys Inc·Product code LNH·October 12, 2005

    BONE-LOK PLS IMPLANT

    FDA Adverse Event
    Malfunction ·INTERVENTIONAL SPINE, INC.·Product code MRW·February 28, 2011

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026