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

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    HOVERROUND TEKNIQUE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HEX-FIX

    FDA UDI
    Smith & Nephew, Inc.·03596010069412·TITANIUM HALF PIN 5.0MM X 20MM

    ArgenZ HT+ 95x14 C4

    FDA UDI
    ARGEN CORPORATION, THE·D818122707·Dental porcelain/ceramic restoration kit

    GENERATION C AESTHETIC SELF-LIGATING BRACKET SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    LIQUICHEK URINE TOXICOLOGY CONTROL LEVEL S1E, MODEL 438; LEVEL S2E, MODEL 439

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 21, 2013

    HP MBT CEM KEEL PUNCH SZ 4-7

    FDA Adverse Event
    Malfunction ·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code LXH·September 26, 2014

    UNKNOWN DEPUY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·June 3, 2011

    STEM EXTRACTOR F/GUIDE BAR NO. 03.401.07

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code HWB·February 2, 2017

    Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder implants.

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·May 2, 2018

    Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000

    FDA Enforcement
    Class I ·Ongoing·Covidien·November 8, 2023