BEUDAMED
    9 results · 20ms · 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.

    CANON AUTOREFRACTOMETER R-22

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Snowden-Pencer

    FDA UDI
    STERIS CORPORATION·10885403152375·Snowden-Pencer RASPS PEET 19CM 7-1/2 inches, ST...

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172972410·

    TRUELOK EVO

    FDA UDI
    ORTHOFIX SRL·18052469472026·TRUELOK EVO RX FOOTPLATE D200MM STERILE

    iSee (roflufocon D, roflufocon E) Daily Wear Orthokeratology Contact Lenses

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    X-CAL

    FDA 510(k)
    FDA Class 2 ·Hematology

    SECNDRY SET 34IN NDEH W/EXT HOOK

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·May 23, 2014

    PLMA DVC V11.51 1 N

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·October 20, 2010

    TI MATRIX LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code NKB·December 21, 2012