BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    SIS WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    artegral HD

    FDA UDI
    Merz Dental GmbH·D7091973170·posteriors; shade BL2; size XL; upper jaw

    R-PORT II LAPAROSCOPIC ACCESS DEVICE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Epicardia Anywhere

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RINGLOC-X E1 STD 58/36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·February 21, 2013

    RELIANCE TRANSFER CART

    FDA Adverse Event
    STERIS CANADA CORPORATION·Product code LDS·January 28, 2011

    JAGWIRE?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code EZB·August 1, 2014

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 433170.

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