BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    I.V. PRO

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PROSTHETIC CEMENT REMOVER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORAMAGICRX ORAL WOUND RINSE

    FDA 510(k)
    FDA Unclassified ·Unknown

    ASR ACETABULAR IMPLANT 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 22, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    BIOMET StageOne, Shoulder Cement Spacer Mold 10 MM, 50 X 21 X 57 MM, Silicone, Sterile, Item 431410.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020