BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    MOELLERS DECARBOXYLASE, ONITHINE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517302090·Archon Screw, 4.0x19mm S.D. Fixed Recon

    ASP GLOBAL

    FDA Adverse Event
    Malfunction ·ASP GLOBAL·Product code FRL·March 21, 2020

    NEBULIZER, DISP, 2D0815

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CLEARSCAN

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEROYAL ESMARK BANDAGES

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES·Product code FQM·March 17, 2020

    TERUMO PERFUSION SYSTEM 9000

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·October 13, 2010

    FORTIFY DR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014

    DEPUY ASR XL FEM IMP SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 19, 2012

    Exactech Equinoxe CAGE GLENOID, CEMENTED, beta curvature, Mates with: a) 47, 50, 53 head, Medium, Item Number 314-13-13, b) 47, 50, 53 head, Large, Item Number 314-13-14, c) 47, 50, 53 head, Extra Large, Item Number 314-13-15; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024