BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    COONRAD/MORREY ELBOW CEMENT RESTRICTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319718223·Probe and Excavator, 6" blunt

    Myo/Wire II

    FDA UDI
    A & E MEDICAL CORPORATION·10841291101970·SS Suture, 6 per sleeve

    PRODUCTOS FAMILIA S.A.

    FDA registration
    PRODUCTOS FAMILIA S.A.·1 product·🇨🇴 Colombia

    BIOMEDICS 52 (OCUFILCON B) UV BLOCKING DAILY WEAR SOFT CONTACT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CHAD THERAPEUTICS OXYMATIC MODEL 401 AND OXYMATIC MODEL 411

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    COMPLETE

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LPN·April 17, 2020

    BIOMEDICS 1 DAY (52%) STRIP (OCUFILCON B)

    FDA Adverse Event
    Injury ·COOPERVISION CARRIBEAN CORPORATION·Product code MVN·August 29, 2019

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·April 8, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 15, 2011

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 7, 2008

    CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 (21-2120, 21-2125, and 21-2127) Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of infusion, intermittent bolus, and/or with patient-controlled demand doses.

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·August 14, 2024