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

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    Tigon Medical Gryphon Anchor Line

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NA

    FDA UDI
    DEPUY MITEK, LLC·10886705007370·Cortical Screw 4.5mm x 64mm

    Blade Scalpel

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113479·MINIATURE BLADE #64 (BX/5)

    INNESIS PEEK CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SANIDAD FAR-INFRARED MINI LAMP, MODEL FI-3646

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VERSACROSS CONNECT LAAC ACCESS SOLUTION

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023

    PRIMARY IV PLUMSET

    FDA Adverse Event
    Malfunction ·HOSPIRA·Product code FPA·August 17, 2011

    TEXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code MAF·November 4, 2008

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013

    VERSACROSS CONNECT LAAC ACCESS SOLUTION

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·April 25, 2023