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

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    CRYO-TOUCH III

    FDA 510(k)
    FDA Class 2 ·Neurology

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00763000889081·SCREW 3120415 4.0 X 15 SELF DRILL FIX

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994235114·SCREW 3120415 4.0 X 15 SELF DRILL FIX

    NOVO Health Services, LLC

    FDA UDI
    NOVO HEALTH SERVICES, LLC·00810019800948·Sheet, Three Quarter

    NOVO Health Services, LLC

    FDA UDI
    NOVO HEALTH SERVICES, LLC·00812564030627·THREE QUARTER SHEET

    N/A

    FDA UDI
    Tyber Medical, LLC·M695M1204150·

    Viper

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·00816734021729·Fixed Wire Balloon Dilator

    SIGNATURE PLANNER / SIGNATURE GUIDES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACUPULSE 30/40 ST CO2 LASER SYSTEM AND ACUPULSE 40WG CO2 LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDTRONIC SCREW 3120415

    FDA Adverse Event
    Injury ·MEDTRONIC ENGINEERING AND INNOVATION CENTER (MEIC)·Product code KWQ·October 16, 2023

    MEDTRONIC PLATE 7200060

    FDA Adverse Event
    Injury ·MEDTRONIC ENGINEERING AND INNOVATION CENTER (MEIC)·Product code KWQ·October 16, 2023

    MEDTRONIC SCREW 3120516

    FDA Adverse Event
    Injury ·MEDTRONIC ENGINEERING AND INNOVATION CENTER (MEIC)·Product code KWQ·October 16, 2023

    HF-RESECTION ELECTRODE, FOR TURIS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·February 9, 2023

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, MEDIUM, 12°

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 4, 2024

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 26, 2014

    MULTI-LINK RX VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MAF·June 10, 2011

    HF-RESECTION ELECTRODE, LOOP

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·March 28, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAS·December 28, 2022

    THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·June 6, 2018