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

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    DOCTOR'S NIGHTGUARD

    FDA 510(k)
    FDA Unclassified ·Unknown

    SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC SUSCEPTIBILITY PLATE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    UNITIP GASTROINTESTINAL PRESSURE SENSOR CATHETER

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

    SYSTEM 2S

    FDA Adverse Event
    STERIS MEXICO, S. DE R.L. DE C.V.·Product code FLE·April 11, 2013

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·March 17, 2011

    SIMPLEX P - CE FULL DOSE 10-PK

    FDA Adverse Event
    STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·May 27, 2008

    Thermalon Back Wrap, Item Number 24312

    FDA Enforcement
    Class II ·Ongoing·Bruder Healthcare Company, LLC·April 3, 2024

    Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026

    Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026

    COMP RVRS 25MM BSPLT HA+ADPTR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·July 5, 2023

    UNKNOWN GLENOSPHERE TAPER ADAPTER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·July 5, 2023