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

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    Elevate Moisturizing Spray

    FDA 510(k)
    FDA Unclassified ·Unknown

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486018269·MCK PF INS TRAY SIZE 8 CADDY

    Oticon

    FDA UDI
    Oticon A/S·05707131285089·NERA2 PRO, DESIGNRITE 10 WL CBE

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100011·BARRAQUER WIRE SPECULUM LARGE WITH TABS

    SMITH'S PORTEX NEEDLE-PRO EDGE SAFETY DEVICE WITH

    FDA Adverse Event
    Malfunction ·SMITH'S MEDICAL ASD, INC·Product code FMF·February 8, 2007

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    12-LEAD RESTING ELECTROCARDIOGRAPH, MODELS CP100 & CP200

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 7, 2014

    EON C

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 30, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012