BEUDAMED
    8 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.

    LINE CHARGER MODEL LC-100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR27720531·DuoForce wires max. .021"x.025"

    MIRROR, LARYNGEAL

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    SMARTBLOCK PAIN PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 1, 2007

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 2, 2014

    SCULPTRA

    FDA Adverse Event
    Injury ·AVENTIS PHARMA GRUPPO LEPETIT S.R.L.·Product code LMH·October 1, 2012

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·February 13, 2020