BEUDAMED
    1,558 results · 67ms · 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 ×

    VivaGuard® HA-650 Non-Contact Infrared Forehead Thermometer

    FDA UDI
    Able Diagnostics Inc·00853483008250·Accurate and Quick: (1) Advanced infrared techn...

    VivaGuard

    FDA UDI
    Able Diagnostics Inc·00853483008021·VivaGuard Lancets 50s (30G)

    VivaGuard Ino

    FDA UDI
    Able Diagnostics Inc·00853483008175·VivaGuard Ino Control Solution 2 (1 bottle/kit)

    VivaGuard Ino Smart

    FDA UDI
    Able Diagnostics Inc·00853483008236·VivaGuard Ino Smart Blood Glucose Meter Only Kit

    VivaGuard Ino

    FDA UDI
    Able Diagnostics Inc·00853483008199·VivaGuard Ino Control Solution (1 & 3)

    VivaGuard Ino

    FDA UDI
    Able Diagnostics Inc·00853483008182·VivaGuard Ino Test strips 50s (50s/vial)

    VivaGuard Ino

    FDA UDI
    Able Diagnostics Inc·00853483008052·VivaGuard Ino Blood Glucose Meter Only Kit

    VivaGuard Ino

    FDA UDI
    Able Diagnostics Inc·00853483008151·VivaGuard Ino Blood Glucose Meter

    VivaGuard Ino

    FDA UDI
    Able Diagnostics Inc·00853483008007·VivaGuard Ino Blood Glucose Monitoring System

    VivaGuard

    FDA UDI
    Able Diagnostics Inc·00853483008038·VivaGuard Lancing Device

    VivaGuard

    FDA UDI
    Able Diagnostics Inc·00853483008144·VivaGuard Lancets 100s (30G)

    VivaGuard Ino Smart

    FDA UDI
    Able Diagnostics Inc·00853483008243·VivaGuard Ino Smart Blood Glucose Meter

    VivaGuard Ino

    FDA UDI
    Able Diagnostics Inc·00853483008076·VivaGuard Ino Control Solution (L, M, H, 1 bott...

    VivaGuard

    FDA UDI
    Able Diagnostics Inc·00853483008137·VivaGuard Safety Lancets (100s)

    VivaGuard Ino

    FDA UDI
    Able Diagnostics Inc·00853483008014·VivaGuard Ino Test strips 50s (25s/vial)

    0.8% RESOLVE PANEL B

    FDA Adverse Event
    Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code MWN·August 10, 2009

    0.8% RESOLVE PANEL B

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code MWN·May 8, 2009

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code MMH·August 20, 2013

    BINAXNOW COVID-19 AG SELF TEST 2CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 28, 2023

    ID NOW COVID-19 2.0 TEST KIT 24T OUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 27, 2023