BEUDAMED
    26 results · 23ms · Sources: EU EUDAMED, US FDA

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    S4 CERVICAL OCCIPITAL PLATE SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PGI

    FDA UDI
    Nuvasive, Inc.·00887517419903·PGI Curette, Left Angled

    Duette™

    FDA UDI
    POIESIS MEDICAL, LLC·10852732004088·14FR Duette™ Indwelling Urinary Catheter Urine ...

    Vilex Guidewire

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731120342·Guidewire 1.4x100mm Sgl Trocar

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450173909·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450136799·

    CTC DVT-1 CALF GARMENT, MODEL DVT-1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENA EIA KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 17, 2023

    LARGE PATCH LEAD L67

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code LWS·November 7, 1997

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·April 18, 2023

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 28, 2025

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code OYC·March 1, 2018

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code LFR·May 22, 2007

    CAPSUREFIX NOVUS LEAD MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO VILLALBA·Product code DTB·May 21, 2026

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·June 28, 2017

    PAINSMART

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 29, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·May 12, 2011

    ULTRACISION DISSECT HOOK 10CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC (CINCINNATI)·Product code LFL·August 5, 2008

    EQUINOXE CAGE GLENOID M, POST AUG, RIGHT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·August 7, 2023