BEUDAMED
    9 results · 23ms · 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.

    VELCOM-100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Legacy™3 Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307102397·3.2mmD x 10mmL, 3.0mmD Platform

    Shoreline™ ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981143930·Trial Rasp, 18x15x10mm, 7 Deg Lordosis

    ATTAIN HYBRID GUIDE WIRES, MODEL GWR419378, GWR419388, GWR419478, GWR419488

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Philips CombiDiagnost R90

    FDA 510(k)
    FDA Class 2 ·Radiology

    LEGACY 3 IMPLANT

    FDA Adverse Event
    Injury ·IMPLANT DIRECT SYBRON MANUFACTURING LLC·Product code DZE·September 18, 2019

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2014

    REVEAL DX

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DSI·October 9, 2010

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 10, 2012