BEUDAMED
    9 results · 27ms · 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.
    Filters Regulation: Us FDA ×

    DORSAL COLUMELLA IMPLANT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704267419·

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123007·K-WIRE - SINGLE TROCAR 1.6mm DIA x 150mm

    VIASPAN

    FDA Adverse Event
    Other ·FRESENIUS KABI AUSTRIA GMBH·Product code KDL·March 26, 2012

    OPTILINK(TM) LPM (LASER POWER MODULATOR)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ABL505 BLOOD GAS & ELECTROLYTE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FRN·May 7, 2014

    TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MM X 25MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HWC·February 5, 2013

    REALIZE ADJ GASTRIC BAND-C

    FDA Adverse Event
    Malfunction ·OBTECH MEDICAL SARL_·Product code LTI·January 3, 2011