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.
    Filters Regulation: Us FDA ×

    POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N/A

    FDA UDI
    Key Scientific Products Incorporated·00850041798028·PEP REAGENT

    N/A

    FDA UDI
    Key Scientific Products Incorporated·00850041798042·Pep ReagentT

    CHAPERON GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SUNSHADES, ACRYLIC LENSES, ORDER #SG-01

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 25, 2013

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·February 9, 2011

    ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·August 6, 2014