BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    Dermatac Drape

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

    ambIT*

    FDA UDI
    Avanos Medical, Inc.·00193494001254·ambIT* Pain Control Kit - Male Luer Cassette wi...

    ambIT

    FDA UDI
    SUMMIT MEDICAL PRODUCTS, INC.·00857595005961·ambIT Kit with Male Filter Cassette

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113578·PRESET 600 MICRON KNIFE (BX/5)

    Ti-one 101

    FDA UDI
    HUNG CHUN BIO-S CO., LTD.·04719871590553·Abutment Ø6.5, 6.0 mm Abt. H The Ti-one 101 Den...

    WORKBENCH BY <GENX>

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    TRINITY WRINKLE REMOVER

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

    ADVIA CENTAUR TOTAL HCG (THCG)

    FDA Adverse Event
    Other ·SIEMENS HELATHCARE DIAGNOSTICS, INC.·Product code JHI·October 30, 2008

    M SERIES

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

    OT VERIO IQ 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