BEUDAMED
    14 results · 22ms · 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.

    HEP-2-CRITHIDIA LUCILIAE ANA TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517367389·CoRoent Small, 11x11x14mm 5° Lordotic

    Cabo

    FDA UDI
    Seaspine Orthopedics Corporation·10889981122515·Diameter 4.3mm Fixed Self Tapping Screw, 14mm

    Cabo™

    FDA UDI
    NEUROSTRUCTURES, INC·00841508104056·Fixed - 4.3mm Self Tapping 14mm

    A-FIT®

    FDA UDI
    Gc Orthodontics America Inc.·E53581171400001·A-FIT® 2. MOLAR UPR RGT SZ 14

    BIPAP PRO BI-LEVEL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HAIRMAX DUAL 12

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 15, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code MCX·August 23, 2010

    MEDTRONIC LEAD

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·October 25, 2024

    MEDTRONIC IPG

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·October 25, 2024

    MEDTRONIC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·October 25, 2024

    MEDTRONIC IPG

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code NVZ·October 25, 2024