BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    IPL Hair Removal Device (DE03A-W, DE03A-P, DE03A-V, DE03A-G, DE03B-W, DE03B-P, DE03B-V, DE03B-G)

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

    Stryker Orthopaedics Acetabular Shells, Femoral Stems and Total Hip Instruments for use with the Direct Superior Approach

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO: PNEUTON VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    3/32" END PERF SILICONE DRAIN WITH TROCAR

    FDA Adverse Event
    Malfunction ·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code GCY·November 21, 2008

    ATLAS PLUS VR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 11, 2011

    ADVIA CENTAUR XP

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·July 23, 2013

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·February 20, 2026

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·January 23, 2026

    CR TIBIAL INSERT SZ 2, 9MM, SLOPE ++

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 3, 2024

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·June 25, 2025

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·January 23, 2026

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·January 29, 2026