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

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    DENVER ASCITES SHUNTS, DENVER ASCITES SHUNT PERCUTANEOUS ACCESS KITS

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

    artegral HD

    FDA UDI
    Merz Dental GmbH·D7091973129·posteriors; shade C4; size XS; lower jaw

    PRECICE System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CARBON DIOXIDE REAGENT KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·June 27, 2019

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 5, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 21, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code NIQ·January 28, 2011

    Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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