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

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    MARTIN-LEWIS AGAR

    FDA 510(k)
    FDA Class 2 ·Microbiology

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099860·MN 2ND BI BD KT N/L R/L 176

    MGB Alert® EBV Primer Mix ASR - 480 Reactions

    FDA UDI
    Elitechgroup Mdx LLC·03661540951299·"MGB Alert® EBV Primer Mix contains chemically ...

    Falcon

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730088673·Utility Arch Pliers

    Elite Orthopaedics

    FDA UDI
    Elite Orthopaedics, Inc.·00816591013400·Adjustable Elbow Brace, Right

    Elite Orthopaedics

    FDA UDI
    Elite Orthopaedics, Inc.·00816591013394·Adjustable Elbow Brace, Left

    ACUMED

    FDA UDI
    Acumed LLC·10806378041303·Metacarpal Lkg Plate Targ. Guide, Right

    IMPACT MODULAR TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INSTARAD

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNKNOWN- UNSPECIFIED BY COMPLAINANT

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·April 3, 2014

    ADVIA CENTAUR CP

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·October 22, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 28, 2007

    Rusch/MMG Urinary Catheterization System, 14 Fr; the single use sterile kit contains a Rusch/MMG Intermittent Catheter, gauze tissue, povidone iodine swabs, two vinyl gloves and underpad; 100 kits per box; Rusch, 2450 Meadowbrook Pwy, Duluth, GA 30096, Assembled in Mexico from U.S. Components; product number RLA-142-3

    FDA Recall
    Terminated ·Teleflex Medical·Product code FCM·July 11, 2005

    Weck, DuraHook", Catalog #382800, 1/4" (6mm) Neuro Elastic Retractors, Sterile, Rx only.

    FDA Recall
    Terminated ·Telefelx Medical·Product code GDG·May 12, 2008

    Conditional Fiber Optic Laryngoscope Kit, which contains laryngoscope blades, handles and 2 battery packs for use in Magnetic Resonance environments; Distributed by Teleflex Medical, Research Triangle Park, NC 27709; catalog number 005852300

    FDA Recall
    Terminated ·Teleflex Medical·Product code CCW·March 1, 2007

    Weck, DermaHook", Catalog #382805, 1/2" (12mm) Neuro Elastic Retractors, Sterile, Rx only, Weck Closure Systems, 2917 Weck Drive, Research Triangle Park, NC 27709

    FDA Recall
    Terminated ·Telefelx Medical·Product code GDG·May 12, 2008

    Green Spec Fiberoptic Laryngoscope Handle - Stubby/Short; a battery operated fiberoptic laryngoscope handle for use with green coded fiberoptic systems and single use laryngoscope blades; Teleflex Medical, Bannockburn, IL 60015; catalog number 004413300

    FDA Recall
    Terminated ·Teleflex Medical·Product code CCW·June 15, 2006

    Sheridan Preformed Cuffed Oral Tracheal Tube, 5.0 mm; a Rx, sterile, single use tracheal tube; Hudson Respiratory Care Inc., Temecula, CA 92589-9020, Manufactured in Mexico; catalog number (REF) 5-22210

    FDA Recall
    Terminated ·Teleflex Medical·Product code BTR·September 27, 2006

    Sheridan T.T.X. Tracheal Tube Exchanger, Large Size for tracheal tube sizes 7.5 mm - 10.0 mm; a Rx, sterile, single use tracheal tube exchanger; Hudson Respiratory Care Inc., Temecula, CA 92589-9020, Manufactured in Mexico; catalog number (REF) 5-24006

    FDA Recall
    Terminated ·Teleflex Medical·Product code LNZ·September 27, 2006

    Sheridan Preformed Uncuffed Oral Tracheal Tube, 3.0 mm; a Rx, sterile, single use tracheal tube; Hudson Respiratory Care Inc., Temecula, CA 92589-9020, Manufactured in Mexico; catalog number (REF) 5-22006

    FDA Recall
    Terminated ·Teleflex Medical·Product code BTR·September 27, 2006