BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    S.I.N. Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471130500·K-WIRE - DOUBLE TROCAR WITH GUIDE 0.9mm DIA x 1...

    MICRO I

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    REPROCESSED VESSEL SEALER

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

    Versa-Fx® II Femoral Fixation System

    FDA UDI
    Zimmer, Inc.·00889024036895·

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·October 6, 2008

    HUDSON ISO-GARD FILTER STR. STERILE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAH·June 21, 2013

    EON RECHARGEABLE IPG

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 21, 2011

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 14, 2023