BEUDAMED
    23 results · 22ms · Sources: EU EUDAMED, US FDA

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    Venner PneuX™ ETT (Endotracheal Tube) 6 mm, Venner PneuX™ ETT (Endotracheal Tube) 7 mm, Venner PneuX™ ETT (Endotracheal Tube) 8 mm, Venner PneuX™ ETT (Endotracheal Tube) 9 mm

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583033167·ET20, KIT 10 NFM 75 BE ENCHANT 20

    ECHO BI-METRIC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304492257·

    Echo® Bi-Metric® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868260667·

    GALILEO® LEFTY TIGHTY™ CRT²™ LAG SCREW, LEFT, 10.5mm x 120mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665036596·

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198482·AK3 Ultra Insert Trial Size 1, 20mm

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365120862·

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780419129·Integra® Miltex® Wullstein Ear Forceps 3-1/8" S...

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111017·SILICONE MAT FOR INSTRUMENT CADDY

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973107965·TRIAL 90-SRK-192120 POLY-MPCS 1X20 LEFT

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819212000201·EXMRC MBT 022/UR2 10T 8A

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819212000101·EXMRC Roth 022/UR2 8T 9A

    EXPERIENCE

    FDA UDI
    Gc Orthodontics America Inc.·D78819212000071·Exp CCO RH 022/UR2 10T 9A

    DIAZYME D-DIMER ASSAY KIT,CALIBRATOR SETAND CONTROL SET

    FDA 510(k)
    FDA Class 2 ·Hematology

    NIPPV SILICONE FACE MASK, NIPPV ECONOMY FACE MASK, NIPPV SILICONE NASAL MASK MODEL 10212, 10222, 10202

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DUETTO MT

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM S.P.A.·Product code GEX·April 14, 2022

    LEFTY TIGHTY LAG SCREW, Ø10.5MMX120MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HSB·June 19, 2024

    GALILEO® LAG SCREW INSERTER

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HSB·June 19, 2024

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·October 7, 2008

    UNKNOWN DEPUY ACETABULAR LINER

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code KWA·June 27, 2013