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

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    Hybrid C70

    FDA 510(k)
    FDA Class 2 ·Dental

    Ballard* Closed Suction System for Adults

    FDA UDI
    Avanos Medical, Inc.·00609038944999·BALLARD* Closed Suction System for Adults, T-Pi...

    AARON ARTHROSCOPY ELECTRODE, CATALOG NUMBERS AR00, AR01, AR02, AND AR03

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SOMATOM DEFINITION EDGE

    FDA 510(k)
    FDA Class 2 ·Radiology

    KIT PREFILL NEB W NEB CAP STERILE WATER

    FDA Adverse Event
    Injury ·VYAIRE MEDICAL, INC·Product code OGG·June 29, 2017

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 18, 2011

    BIOGLUE SURGICAL ADHESIVE

    FDA Adverse Event
    Other ·CRYOLIFE, INC.·Product code MFI·October 30, 2008

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 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