BEUDAMED
    9 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.
    Filters Regulation: Us FDA ×

    BLOWER/MISTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Polystar Selection EDITION HD

    FDA UDI
    Merz Dental GmbH·D7091983135·posteriors; shade BL1; size S; lower jaw

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024364868·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024364875·

    PTI HEART-LIFT(TM) CARDIAC ELEVATOR (STERILE)

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    MODIFICATION TO CHILLBUSTER PORTABLE ELECTRIC BLANKET , MODEL 8002

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 28, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 6, 2014

    ALUMINA

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, ORTHOPEDICS·Product code LPF·February 10, 2011