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

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    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·FoundationFocus CDxBRCA

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·FoundationFocus CDx BRCA HRD

    DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169502444·PLATE 2160018 ALIF PLATE 18MM

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075022705·KLEOS PSL METAL MBT 022 UR45 HK PK5 UNI

    Humeris Shoulder

    FDA UDI
    FX SOLUTIONS·03701037304587·HUMERIS STEM TA6V SIZE 18 CEMENTLESS Ti/HA

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694035620·Adjustable Parallel Drill Guide, 6.5/7.3mm

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707016946·CALIBRA 1ST MOLAR BANDS n.LR 18

    Arrow Quickflash Arterial Catheterization Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code MJO·April 9, 2012

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code MJO·April 9, 2012

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code MJO·March 20, 2012

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code MJO·March 20, 2012

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·PIPELINE EMBOLIZATION DEVICE

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·PRESTIGE CERVICAL DISC SYSTEM

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code MJO·February 11, 2022

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code MJO·February 11, 2022

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code MJO·March 31, 2019

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 10, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

    XPERT SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR SWITZERLAND·Product code FGE·September 12, 2008