BEUDAMED
    43 results · 56ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    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...

    NON-ALLERGAN BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·March 2, 2024

    UNK MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURER·Product code FWM·April 20, 2023

    BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·March 1, 2023

    VASCULAR SOLUTIONS DUETT SEALING DEVICE

    FDA Adverse Event
    Death ·VASCULAR SOLUTIONS, INC.·Product code MGB·February 6, 2002

    SINGLE USE ASPIRATION NEEDLE NA-U401SX

    FDA Adverse Event
    Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FCG·March 3, 2022

    ZILVER PTX 35 DRUG-ELUTING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code NIU·November 3, 2017

    MAMMOTOME REVOLVE ST HOLSTER

    FDA Adverse Event
    Injury ·DEVICOR MEDICAL PRODUCTS INC·Product code KNW·December 27, 2023

    VASOSEAL ES

    FDA Adverse Event
    Injury ·DATASCOPE CORP./COLLAGEN PRODUCTS·Product code MGB·April 12, 2000

    UNK MAMMARY IMPLANT

    FDA Adverse Event
    Death ·UNKNOWN MANUFACTURER·Product code FWM·March 11, 2026

    PALMAZ BLUE .018 TRANSPHEPATIC BILIARY STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·January 27, 2009

    PALMAZ BLUE .018 TRANSHEPATIC BILIARY STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·January 27, 2009

    NOGA-STAR DIAGNOSTIC CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code DRF·September 19, 2008

    CAREFUSION THORA / PARA 5F NON-VALVED CATHETER DRAINAGE T

    FDA Adverse Event
    Injury ·CAREFUSION / BD·Product code JOL·March 28, 2019

    CAREFUSION THORA/PARA 5F NON-VALVED CATHETER DRAINAGE T

    FDA Adverse Event
    Injury ·CAREFUSION 2200, INC·Product code JOL·March 26, 2019

    SPIDER FX

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NTE·September 19, 2022