BEUDAMED
    11 results · 18ms · 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.

    QUITETIP

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Modulus Expandable

    FDA UDI
    Nuvasive, Inc.·00195377056061·MOD-EX PL Trial, 11x9mm

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981109·anteriors; shade A4; mould CM2

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930798110910·Stainless Frazier Suction 9FR 10" from bend

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93079811091C0·Frazier Suction Tubes 9FR 260mm from Bend

    Octane A

    FDA UDI
    Choice Spine, LP·10885862166562·

    CORONIS 5MP MAMMO SL, MODEL MDMG 6121

    FDA 510(k)
    FDA Class 2 ·Radiology

    FORCEPS, ELECTROSURGICAL

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ALARIS PUMP MODULE

    FDA Adverse Event
    Injury ·CAREFUSION CORPORATION·Product code FRN·February 20, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 8, 2011

    PROMUS ELEMENT? PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·August 5, 2014