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

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    Anterior Spine Truss System – Stand Alone (ASTS-SA) Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Splintastik

    FDA UDI
    Preat Corporation·00842092169988·Splintastik Refill SM (6-Pack)

    Paradigm

    FDA UDI
    Proprio, Inc.·00850042604045·Paradigm Dynamic Reference Frame

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377045256·RELINE-O Trial, 6mm H Lamina N L-pop

    Lapiplasty SpeedPlate

    FDA UDI
    Treace Medical Concepts, Inc.·00810111221214·Inserter Cap

    JEWELERS PRECISION FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896059320·JEWELERS PRECISION FORCEPS CURVED TIPS #7 SERRA...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694005562·1.3mm Pilot Drill, J-Latch, 12mm

    Sequel Medical

    FDA UDI
    Sequel Medical Inc.·00810071321153·6 Tab Full Ring 220mm

    OptumSI Implant System

    FDA UDI
    SI Solutions, LLC·00850057247022·Blunt Guide Pin

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694066129·1.6 System 1.3mm Pilot Drill J-Latch Sterile Qty 2

    MODEL P-33, BATTERY OPERATED, THREE WHEEL, POWER SCOOTER , MODEL P-33

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MAGNA 5000 PHASED ARRAY CTL SPINE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555242200002·Sounder, Curved, Small

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555112200002·Sounder, Straight

    Clarius Ultrasound Scanner

    FDA UDI
    Clarius Mobile Health Corp·07540205000533·Clarius brand Charger

    Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·EPi-Sense Guided Coagulation System

    COMPRESSURE FRACTURE REPAIR IMPLANT

    FDA Adverse Event
    Injury ·USI ORTHOPAEDICS LLC DBA U.S. ORTHOPAEDICS·Product code HTN·April 6, 2011

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 2, 2014

    Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·EPi-Sense Guided Coagulation System and EPi-Sense ST Coagulation System

    Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·EPi-Sense Guided Coagulation System