BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    QUANTUM EDGE PEDIATRIC DEFIRBRILLATION ELECTRODES

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970391·anteriors; shade D2; mould IM

    ANSiStim-PP

    FDA 510(k)
    FDA Unclassified ·Unknown

    ELECSYS PTH TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·February 20, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 25, 2011

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·July 31, 2014

    ZILVER PTX 35 DRUG-ELUTING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code NIU·September 12, 2017

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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