BEUDAMED
    8 results · 35ms · 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.

    MODEL 3000 HYPERBARIC CHAMBER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    COLLAGEN DURA MEMBRANE

    FDA 510(k)
    FDA Class 2 ·Neurology

    C-VUE 55 TORIC (METHAFILCON A) MULTIFOCAL CONTACT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LOGIC FEMORAL PS CEM RIGHT SZ 5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 6, 2024

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 30, 2014

    POROUS NEXGEN TM PATELLA, 38MM DIA.

    FDA Adverse Event
    Injury ·ZIMMER TMT·Product code JWH·June 9, 2015

    SOFTCLIX® PLUS LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·September 22, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018