BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    Q Pedicle Instruments

    FDA 510(k)
    FDA Class 2 ·Neurology

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668101377·DIAMOND STEP KNIFE TRI-FACET

    3M Attest Rapid Readout Biological Indicator

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 30

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OT VERIO IQ METER

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

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 22, 2011

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 1, 2013

    BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·April 21, 2021