BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    BACT/ALERT FAN CULTURE BOTTLES

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ALIF

    FDA UDI
    Nuvasive, Inc.·00887517839756·ALIF Blade, 140mm Narrow

    SABOURAUD DEXTROSE SD EMMONS MOD. AGAR SLT TUBE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    LEGION POROUS PRIMARY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENDOPATH ENDOSCOPIC MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·June 25, 1997

    PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBH·October 20, 2025

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·February 21, 2013

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·August 1, 2014

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 5, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 6, 2017