BEUDAMED
    8 results · 19ms · 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.

    NOVA LITE TM THYROID

    FDA 510(k)
    FDA Class 2 ·Immunology

    INSITE STEERABLE GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STAT FAX(TM)-2100

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    BD PLASTIPAK 50ML LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·September 11, 2019

    PATIENT INTERFACE 8253200 RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC INC·Product code ETN·January 9, 2013

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·November 12, 2010

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·July 1, 2014

    BD PLASTIPAK LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 1, 2019