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

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    iTotal Posterior Stabilized (PS) Knee Replacement System, iTotal Cruciate Retaining (CR) Knee Replacement System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    X-CORE

    FDA UDI
    Nuvasive, Inc.·00887517424235·X-CORE 2 Ti Core, Ø16x18-25mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031592·Washer for 6.5/7.3mm Screws

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075022750·KLEOS PSL METAL MBT 022 LL5 HK PK5

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528108192·Washer, 6.5/7.0mm Screw, Sterile 2Pk

    SLIMPLICITY ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SECTRA MICRODOSE MAMMOGRAPHY

    FDA 510(k)
    FDA Class 2 ·Radiology

    Widex

    FDA UDI
    Widex A/S·05706069898088·WIDEX EVOKE E-CIC (Light beige ) 50, Right, RC ...

    Widex

    FDA UDI
    Widex A/S·05706069897791·WIDEX EVOKE E-XP (Light beige ) 50, Telecoil, R...

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·ASTRON PULSAR STENT SYSTEM, PULSAR-18 STENT SYSTEM

    SYRINGE 0.5ML 29GA 1/2IN 200BX CA

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 3, 2021

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 15, 2013

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 23, 2025

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·Astron Pulsar; Pulsar-18; Pulsar-18 T3

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·Astron Pulsar Stent System and Pulsar-18 Stent System

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·Astron Pulsar, Pulsar-18, Pulsar-18 T3

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·Pulsar-18 T3 Stent System

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·Astron Pulsar/Pulsar-18 Stent Systems

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·Astron Pulsar/Pulsar - 18 Stent System

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·Pulsar-18 T3