BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    SUTRASILK SILK SUTURE

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

    NEEDLE*LESS DRUG VIAL ADAPTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GALIX MA-6C HOLTER CASSETTE RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 12, 2015

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 13, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014

    CABLE CUTTER W/TRIGGER HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXZ·February 21, 2024

    TRIGGER HANDLE F/CABLE CUTTER

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXZ·May 18, 2018

    Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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