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

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    PHF20 20 MOBILE C-ARM IMAGE INTENSIFIER

    FDA 510(k)
    FDA Class 2 ·Radiology

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515243293·Sickle Knife, shrp, str, adult

    Ophthalmic Spoon

    FDA UDI
    KATENA PRODUCTS, INC.·00841668104088·B H KIM INTRAOCULAR MIRROR

    TOTAL SHOULDER PROSTHESIS POLYETHYLENE GLENOIND CO

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BELMONT MODEL PBP INTRA-AORTIC BALLOON PUMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CORDLESS DRIVER 3

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HRX·December 14, 2010

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·January 30, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 3, 2014

    VANGUARD FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    VANGUARD TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    CC CRUCIATE TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018