BEUDAMED
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    Advanced Cell Diagnostics, Inc.

    FDA registration
    Advanced Cell Diagnostics, Inc.·2 products·🇺🇸 United States

    RNAscope™ ISH Probe Kappa

    FDA UDI
    Advanced Cell Diagnostics, Inc.·00850042722015·RNAscope™ ISH Probe Kappa is designed to hybrid...

    RNAscope™ ISH Probe SARS-CoV-2

    FDA UDI
    Advanced Cell Diagnostics, Inc.·00850042722008·RNAscope™ ISH Probe SARS-CoV-2 is designed to h...

    RNAscope™ ISH Probe IGLL5

    FDA UDI
    Advanced Cell Diagnostics, Inc.·00850042722039·RNAscope™ ISH Probe IGLL5 is designed to hybrid...

    RNAscope™ ISH Probe Lambda

    FDA UDI
    Advanced Cell Diagnostics, Inc.·00850042722022·RNAscope™ ISH Probe Lambda is designed to hybri...

    FLEXISION

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code EOQ·December 5, 2022

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 26, 2021

    IMPELLA

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·April 29, 2026

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·September 12, 2025

    NONE

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code GCJ·September 8, 2023

    MYNX VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·ACCESSCLOSURE, INC.·Product code MGB·August 14, 2008

    INQUIRY¿ STEERABLE EP CATHETER

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code DRF·May 24, 2023

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·March 21, 2011

    GENESISXP DUAL 4- CHANNEL IPG

    FDA Adverse Event
    Other ·ADVANCED NEUROMODULATION SYSTEMS, INC·Product code LGW·August 6, 2007

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·September 11, 2013

    PRECISE SDS SELF EXPANDING

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·July 2, 2014

    PRECISE SDS SELF EXPANDING

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·July 2, 2014

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·August 24, 2022

    PULSE GEN MODEL 1000

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·December 20, 2024

    PRESSUREWIRE CERTUS INTRODUCER NEEDLE

    FDA Adverse Event
    Death ·Product code DQX·April 4, 2008