BEUDAMED
    26 results · 25ms · Sources: EU EUDAMED, US FDA

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    DANE TECHNOLOGIES WHEELCHAIR MOVER, MODEL WM 2000

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Cook

    FDA UDI
    COOK INCORPORATED·00827002141858·Urethral Dilator Set

    Thermaloy

    FDA UDI
    Rmo, Inc.·00885797018021·THERMALOY(R) PREFORMED IDEAL ARCH MN .014

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180504048·Low Profile Bone Funnel w/ Removable Handle

    S~Curve

    FDA UDI
    COOK INCORPORATED·00827002327894·S-Curve Urethral Dilator Set With AQ, Hydrophil...

    SENTECH MEDICAL EXPRESS COMPRESSION SYSTEM (P/N SM800)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDO-GLIDE

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

    PRECISION MONTAGE MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 18, 2021

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 7, 2021

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 11, 2025

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·March 3, 2025

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 23, 2025

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 27, 2024

    880 HUMIDIFICATION SYSTEM

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·March 31, 2010

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·April 23, 2013

    ACCURUS 800CS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·April 13, 2011

    TRILOGY ACETABULAR SYSTEM SHELL WITH CLUSTER HOLES POROUS

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code KWB·July 1, 2008

    880 HUMIDIFICATION SYSTEM

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD.·Product code BTT·February 15, 2010

    RESPIRATORY HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 12, 2024

    RESPIRATORY HUMIDIFIER

    FDA Adverse Event
    Injury ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·July 4, 2024