BEUDAMED
    9 results · 25ms · 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.

    FIELD TREND

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NexGen® Trabecular Metal®

    FDA UDI
    Zimmer, Inc.·00889024208247·

    NexGen® Trabecular Metal®

    FDA UDI
    Zimmer, Inc.·00889024208254·

    PULMANEX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PUMUCKL AND/OR DIETERLE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    BIOMET BC R 1X40 US

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·June 17, 2024

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 10, 2011

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 23, 2014

    PUMP MMT-715NAS PRDGM INS V2.1 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·October 24, 2007