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

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    SYNCHRON CX SYSTEMS PHOSPHORUS REAGENT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040114582·HP Intraoral Tips Yellow Small

    WATERLASE AND WATERLASE MD

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

    KWIK-AWA VEST

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPIROPERFECT

    FDA Adverse Event
    Malfunction ·MEDIKRO OY·Product code BZG·August 11, 2023

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 4, 2013

    COAGUCHEK® S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·January 27, 2011

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 31, 2014

    CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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