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

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    HEMOCUE HEMOGLOBIN CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Hematology

    OXYLOG 2000 PLUS SYSTEM (MODEL 5705080), OXYLOG 2000 PLUS BASIC DEVICE (MODEL 5705082)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Powder Free Nitrile Examination Glove, Tested for Use with Chemotherapy Drugs (Blue)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 19, 2014

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIVISION·Product code INK·October 22, 2010

    PINNACLE PELVIC FLOOR REPAIR KITS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·December 20, 2012

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026