BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    MRIaudio PREM System with MRIview

    FDA 510(k)
    FDA Class 2 ·Radiology

    Pulse® CR Pink

    FDA UDI
    INNOVATIVE HEALTHCARE CORPORATION·30813172023118·Gloves, Exam, Chloroprene, Non-Sterile, Powder-...

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180543917·MOD SIGMA SHANKDRIVER, LARGER RATCHETING THUMBW...

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·June 16, 2006

    AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LEUCADIA PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EVIS EXERA III DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·February 18, 2022

    OMNIFIX®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FMF·March 6, 2026

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·October 6, 2008

    HUDSON SPIRAL-FLEX ENDOTRACHEAL TUBE, 7.5MM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·June 21, 2013

    NONE

    FDA Adverse Event
    Malfunction ·UNK·Product code GES·July 21, 2011

    Quanta System Sterile Optical Laser Fiber, single use

    FDA Enforcement
    Class II ·Terminated·Quanta System, S.p.A.·June 16, 2021