BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ASEPTEX 1809 FLUID-RESISTANT MOLDED SURGICAL MASK

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

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517312020·Archon Screw, 4.5x18mm S.T. Variable

    Reprocessed Torqr Diagnostic EP Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARGYLE A-V MEDI-WING HEMODIALYSIS SET

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

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·June 18, 2014

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 20, 2012

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·October 20, 2010

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

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