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

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    17HQ901G-B

    FDA 510(k)
    FDA Class 2 ·Radiology

    AESCULAP-MEITHKE PROSA ADJUSTABLE SHUNT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    CarpX

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

    ADVIA CENTAUR TROPONIN ULTRA ASSAY

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS, INC·Product code MMI·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

    PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code LPH·October 17, 2025

    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