BEUDAMED
    11 results · 38ms · 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 ×

    HOWMEDICA ACETABULAR SHELL W/SCREW HOLES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Brasseler USA

    FDA UDI
    Provision·B504OMKM331020·

    Brasseler USA

    FDA UDI
    Provision·00810041064820·

    SeaSpine Spacer System - Pacifica™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981058692·Pacifica Trial, 9mm x 20mm x 9mm

    SeaSpine Spacer System - Pacifica™

    FDA UDI
    Seaspine Orthopedics Corporation·10889910058694·Pacifica Trial, 9mm x 20mm x 9mm

    FLOWER ANKLE PLATING SET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDIC COLON MODEL, RELEASE 1

    FDA 510(k)
    FDA Class 2 ·Radiology

    CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 13, 2022

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Other ·INSULET CORPORATION·Product code LZG·December 11, 2010

    SONCISION

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO HEALTHCARE·Product code LFL·January 25, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 14, 2014