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

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    SSCIMED CORONARY GUIDE WIRE/INFUSION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DILATING TIP TROCAR WITH STABILITY SLEEVE - 12MM DIAMETER

    FDA Adverse Event
    Injury ·Product code GCJ·June 20, 2006

    IDOC UPPER ARM ATTACHED BLOOD PRESSURE AND PULSE RATE MONITOR, MODEL ID-42A/ID-43A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    K2M Fenestrated Tap System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 9, 2013

    VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·January 7, 2011

    LINOX SD 65/16

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVY·July 23, 2014

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

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