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

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    RAPIDONE - OPIATES TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PROCARE

    FDA UDI
    DJO, LLC·00888912037938·FOAM ARM BOARD PADS7.5"X16"X2", 12 PR/BX

    POZZI STANDARD WIRE

    FDA UDI
    AMERICAN TOOTH INDUSTRIES·D772ATI01519908200·POZZI STANDARD WIRE .030

    Aimanfun Lumea Comfort

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

    TRIA HAIR REMOVAL LASER SYSTEM

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

    M2A-MAGNUM 42-50MM TPR INSRT-6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 13, 2019

    UNKNOWN GLOBAL ADV SHOULDER CEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code HSD·March 6, 2013

    PFC SIGMA C/R NPOR FEM LT SZ 3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 8, 2011

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·August 8, 2014

    M2A-MAGNUM MOD HD SZ 42MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 13, 2019

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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