BEUDAMED
    948 results · 23ms · 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 ×

    OLYMPUS

    FDA Adverse Event
    Other ·OLYMPUS·Product code FTJ·June 10, 2003

    OLYMPUS

    FDA Adverse Event
    Other ·OLYMPUS·Product code FTJ·June 10, 2003

    OLYMPUS

    FDA Adverse Event
    Other ·OLYMPUS·Product code FTJ·June 10, 2003

    OLYMPUS

    FDA Adverse Event
    Malfunction ·OLYMPUS OPTICAL CO. LTD.·Product code FDF·February 16, 2001

    OLYMPUS

    FDA Adverse Event
    OLYMPUS AMERICA INC.·Product code FDF·July 21, 2003

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MQR·March 22, 2018

    DIMENSION®

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code CFQ·November 3, 2016

    MTS ANTI-IGG, -C3D CARD

    FDA Adverse Event
    Malfunction ·MICRO TYPING SYSTEMS, INC,·Product code CFQ·May 8, 2009

    VITROS IMMUNODIAGNOSTICS PRODUCTS AHAV IGM REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code CFQ·April 3, 2008

    DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code CFQ·August 1, 2012

    DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code CFQ·August 30, 2012

    DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code CFQ·August 16, 2012

    BN II SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code CFQ·August 31, 2018

    OLYMPUS COLONOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS (UNKNOWN ADDRESS)/ALLEGIANCE HEALTH CARE·Product code FDF·August 28, 2002

    Xpert Xpress Strep A, XPRSTREPA-10, P/N: 302-2294 IVD, Rx Only

    FDA Recall
    Open, Classified ·Cepheid·Product code PGX·April 24, 2023

    Xpert Xpress Strep A, REF:Xprstrepa-CE-10, CE IVD,

    FDA Recall
    Open, Classified ·Cepheid·Product code PGX·April 24, 2023

    Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code: 07332940000158 Xpert SA Nasal Complete kit; 10 test kit: A collection of reagents and other associated materials intended to be used for the direct qualitative and/or quantitative detection of nucleic acid from methicillin-resistant and methicillin-susceptible Staphylococcus aureus (MRSA/MSSA) bacteria present in a clinical specimen, using a nucleic acid technique

    FDA Recall
    Open, Classified ·Cepheid·Product code NQX·August 6, 2025

    Antiserum, Cf, Q Fever

    FDA classification
    FDA Class 1 ·Antiserum, Cf, Q Fever

    Antigen, Cf, Q Fever

    FDA classification
    FDA Class 1 ·Antigen, Cf, Q Fever

    Radioimmunoassay, Immunoglobulins (G, A, M)

    FDA classification
    FDA Class 2 ·Radioimmunoassay, Immunoglobulins (G, A, M)