BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SPECTRANETICS LEAD LOCKING DEVICE (LLD) #1, #2, #3 LISTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ELEVATE PROLAPSE REPAIR SYSTEM WITH PC COATED INTEPRO LITE- APICAL AND POSTERIOR PROLAPSE REPAIR SYSTEM, ANTERIOR AND AP

    FDA 510(k)
    FDA Class 3 ·Obstetrics/Gynecology

    F&P Vitera Mask Full Face A Model (Small, Medium, Large), F&P Vitera Mask Full Face Sleep Lab Model (Small, Medium, Large)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·November 7, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·March 5, 2013

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    EON MINI IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·February 8, 2011

    CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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