BEUDAMED
    17 results · 22ms · Sources: EU EUDAMED, US FDA

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    Implacil Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304270497·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528128213·3.0 X 24mm Cannulated Headed Screw, T10

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A18302480·18mm H x 30mm W x 24mm L x 8 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A183024120·18mm H x 30mm W x 24mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A183024150·18mm H x 30mm W x 24mm L x 15 degrees ALIF

    SECORE C LOCUS SEQUENCING KIT

    FDA Adverse Event
    Malfunction ·LIFE TECH CORP·Product code MZI·January 17, 2014

    MiniSPC Button

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071148201·18F x 3.0cm MiniSPC Low Profile Suprapubic Cath...

    MiniSPC Button

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071150822·18F x 3.0cm MiniSPC Low Profile Suprapubic Cath...

    MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S5 - LATER

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·December 16, 2020

    TORQUE DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HYLATOPIC EMOLLIENT FOAM

    FDA 510(k)
    FDA Unclassified ·Unknown

    MOTO PARTIAL KNEE TIBIAL INSERT FIX S4 LM - 8MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·October 26, 2023

    CORTSCR Ø3.5 L30 TI

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code KWQ·June 21, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 28, 2011

    LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·October 17, 2014

    SMALLBORE TRIFUSE EXT. SET

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·August 16, 2016