BEUDAMED
    11 results · 25ms · Sources: EU EUDAMED, US FDA

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    AST/SGOT LIQUID REAGENT - KINETIC METHOD

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517403803·CoRoent® XL, 16x18x50mm 10°

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981650·anteriors; shade D3 light; mould CM4

    AERONEB GO NEBULIZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TERRY KERATOMETER

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    UMBILICAL CATHETER

    FDA Adverse Event
    Malfunction ·VYGON·Product code FOS·February 17, 2021

    SEE H-10

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·February 27, 2013

    LOCKING INSERT AXSOS 5.0MM LOCKING SET

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code HRS·January 12, 2011

    MIH MOD CUP INSERTER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LXH·August 5, 2014

    Femoral Nail, LEFT T2 GTN ¿12x360 mm, Product Number 18501236S

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·July 18, 2018

    Femoral Nail, A/R T2 Femur ¿12x360 mm, Product Number 18251236S

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·July 18, 2018