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

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    Symbia Pro.specta VA20A Family

    FDA 510(k)
    FDA Class 2 ·Radiology

    Young Dental

    FDA UDI
    YOUNG DENTAL MANUFACTURING I, LLC·00302732311028·TRACE DISCLOSING SOL. 2OZ.

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776204822·SHEPHERD PISHING CURETTE

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111139413·SKLARLITE OP SCISS SS ST 5 1/2

    Intrigue

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573021109·INTRG WHISP ROTH CEN +12T +5A 022 UL

    Curette

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102091·SHEPHERD CAPSULE POLISHER

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946030377·X SERIES ADVANCED, 12 LEAD W/INTERP, PACE, SPO2...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946061982·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 12 LE...

    n/a

    FDA UDI
    Ortho Development Corporation·00822409068081·Slotted Stem Trial 23x110mm

    MICROLAB SPIROMETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FreeStyle Libre 2 Flash Glucose Monitoring System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    IMPL TAPERED SCR-V SBM 3. 7MM 3.5MM 16MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·August 1, 2023

    IMPL TAPERED SCR-V SBM 3. 7MM 3.5MM 16MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·September 7, 2021

    EQUATE

    FDA Adverse Event
    Injury ·ASO LLC·Product code KGX·July 23, 2024

    CONV PN SEC MACRO OL

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD·Product code FPA·October 30, 2008

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·August 26, 2011

    PLUM XLD 110V L.A.

    FDA Adverse Event
    Malfunction ·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·July 12, 2013

    PANEL PHOENIX NMIC ID 208

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·February 24, 2021

    SIGNA Architect AIR, Nuclear Magnetic Resonance Imaging System

    FDA Enforcement
    Class II ·Ongoing·GE Medical Systems, LLC·December 4, 2024

    CARESCAPE Canvas Smart Display, Model Numbers: a) 5700023, b) 5700023-02, c) 5939590-102; monitor, physiological, patient

    FDA Enforcement
    Class II ·Ongoing·GE Healthcare Finland Oy·July 3, 2024