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

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    FDA 510(k)
    FDA Class 2 ·Radiology

    SILTEX MEDIUM HEIGHT TISSUE EXPANDER STYLE 9200, 800CC

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·February 8, 2018

    ACTINOMYCETE DIFFERENTIAL MEDIA

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Tri-Staple 2.0 Reinforced Reload

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·CARROLL HEALTHCARE·Product code FNL·February 21, 2013

    CE INTERMATE SV 100, 48 PACK,50125

    FDA Adverse Event
    Malfunction ·Product code FRN·January 28, 2011

    UNKNOWN DEPUY TI KEELED SZ 3 TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·August 1, 2014

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 433175.

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