BEUDAMED
    24 results · 44ms · Sources: EU EUDAMED, US FDA

    SOS Glenoid Component

    FDA registration
    HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States

    SPECIAL ORTHOPAEDIC SOLUTIONS GLENOID SHOULDER COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

    FDA classification
    FDA Class 2 ·Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

    Hybernite ROC US HHU19018WT0ECBCK

    FDA registration
    PLASTIFLEX HEALTHCARE DIVISION OF PLASTIFLEX GROUP NV·1 product·🇧🇪 Belgium

    Hybernite ROC US HHU19018WT0ECBCK

    FDA registration
    Dongguan Plastiflex Hose Technology Ltd·1 product·🇨🇳 China

    VOCO Paste

    FDA registration
    VOCO GMBH·1 product·🇩🇪 Germany

    LARGE PLATE/WIRE CUTTER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896051454·LARGE PLATE/WIRE CUTTER

    Altus Spine Cervical Interbody Fusion System

    FDA UDI
    Altus Spine, LLC·00843210131184·Rasp, W/Tab

    PMT CORPORATION - STEREOTACTIC

    FDA UDI
    PMT CORPORATION·00650551038719·SILICONE STOPPERS WITH SLIT, FOR DEPTHALON

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·34546540134739·LIGATURE WIRES

    RMS CO.

    FDA registration
    RMS CO.·3 products·🇺🇸 United States

    NICOLET WIRELESS EEG

    FDA registration
    Natus Neurology Incorporated·2 products·🇺🇸 United States

    BACT/ALERT CSR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SIMPLICITY QD SOFT INFUSION SET FOR USE BY PEOPLE WITH DIABETES IN INFUSE INSULIN SUBCUTANEOUSLY FROM A PUMP OR SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LL 100, 103, 104 DIAGNOSTIC LAPAROSCOPE RIGID ROD LENS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Stimulator, Autonomic Nerve, Implanted For Epilepsy

    FDA Pre-Market Approval
    FDA Class 3 ·VNS THERAPY SYSTEM

    Bladeless Trocar (E05, E10, E11, E12, ES05, ES10, ES12)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Stimulator, Autonomic Nerve, Implanted (Depression)

    FDA Pre-Market Approval
    FDA Class 3 ·VNS THERAPY GENERATOR (DEMIPULSE) (ASPIREHC)

    Electric Toothbrush: 1990, 1991, 1992, 1993, 1994, 1995, 1996, 1997, 1998, 1998, 2000, 2001, 2002, 2003, 2004, 2005

    FDA registration
    SHENZHEN SINCO TECHNOLOGY CO., LIMITED.·1 product·🇨🇳 China

    Stimulator, Autonomic Nerve, Implanted For Epilepsy

    FDA Pre-Market Approval
    FDA Class 3 ·VNS THERAPY SYSTEM