BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    MIDDLEBROOK BASED MEDIA

    FDA 510(k)
    FDA Class 1 ·Microbiology

    WALLFLEX ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·January 16, 2025

    WALLFLEX PARTIALLY COVERED ESOPHAGEAL STENT SYSTEM

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

    Octane aspiration system

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·October 18, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 13, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2015

    CONNEC L141 F/INSERTION HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·February 21, 2022

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

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