BEUDAMED
    21 results · 40ms · Sources: EU EUDAMED, US FDA

    CHRISTIAN DIENER GMBH

    FDA registration
    CHRISTIAN DIENER GMBH·1 product·🇩🇪 Germany

    VICTORY

    FDA registration
    GLOBUS MEDICAL, INC.·1 product·🇺🇸 United States

    J&B PRECISION, INC.

    FDA registration
    J&B PRECISION, INC.·1 product·🇺🇸 United States

    VICTORY™ Lumbar Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113318·PHACO KNIFE 1.8MM ANGLED (BX/5)

    Sterigenics US LLC

    FDA registration
    Sterigenics US LLC·2 products·🇺🇸 United States

    VOMA ECZA DEPOSU MEDIKAL URUNLER SAN. TIC. A.S.

    FDA registration
    VOMA ECZA DEPOSU MEDIKAL URUNLER SAN. TIC. A.S.·2 products·🇹🇷 Türkiye

    Marathon™ Flow Directed Catheter

    FDA registration
    MICRO THERAPEUTICS, INC. DBA EV3 NEUROVASCULAR·2 products·🇺🇸 United States

    Marathon™ Flow Directed Catheter

    FDA registration
    MICRO THERAPEUTICS, INC. DBA EV3 NEUROVASCULAR·2 products·🇺🇸 United States

    Light based over-the-counter hair removal

    FDA registration
    DONGGUAN DEFINE BEAUTY ELECTRONIC TECHNOLOGY CO.,LTD·1 product·🇨🇳 China

    Marathon™ Flow Directed Catheter

    FDA registration
    Medtronic Distribution Center·2 products·🇺🇸 United States

    STERIS Corporation de Republica Dominicana, S.R.L.

    FDA registration
    STERIS Corporation de Republica Dominicana, S.R.L.·2 products·🇩🇴 Dominican Republic

    RevitalOx PAA HLD Solution Part B (SL-MF, SLDC-RR)

    FDA registration
    STERIS CORPORATION·1 product·🇺🇸 United States

    ICB/ASX15

    FDA registration
    Integra LifeSciences Corporation·2 products·🇺🇸 United States

    RevitalOx PAA HLD Solution Part B (SL-MF, SLDC-RR)

    FDA registration
    STERIS Corporation·1 product·🇺🇸 United States

    RevitalOx PAA HLD Solution Part B (SL-MF, SLDC-RR)

    FDA registration
    STERIS CORPORATION·1 product·🇺🇸 United States

    MINERVA 58 ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    Marathon Flow Directed Micro Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Appliance, Fixation, Spinal Intervertebral Body

    FDA classification
    FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body

    Catheter, Continuous Flush

    FDA classification
    FDA Class 2 ·Catheter, Continuous Flush