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

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    MultiScan G-Arm System

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517566300·CoRoent Ant TLIF PEEK, 15x11x28mm 0°

    AGXO

    FDA UDI
    Oticon A/S·05707131288158·H330V2, DESIGNRITE 10 WL SOR AGXO

    ProLift

    FDA UDI
    Life Spine, Inc.·00190837117511·

    Crosslink Bonding Adhesives

    FDA UDI
    TP ORTHODONTICS INC·00192029000113·In Preloaded Syringe Natural Color Paste 24 g (...

    Pro Lift Instruments

    FDA UDI
    Life Spine, Inc.·00190837031138·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100257·CHU ASPIRATING SPECULUM SOLID

    HNM SPORTS MEDICINE

    FDA UDI
    HNM STAINLESS, LLC.·00812171029908·ETHOS PRO LABRAL ANCHOR, PEEK, 3.3mm x 6mm, (1)...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575292998·Knee femur prosthesis trial - General Instrument

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575292769·Knee femur prosthesis trial - General Instrument

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575292509·Knee femur prosthesis trial - General Instrument

    MEDCOMP SPLIT CATH II

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HNM SPORTS MEDICINE

    FDA UDI
    HNM STAINLESS, LLC.·00842962103708·ETHOS PRO LABRAL ANCHOR, PEEK, 3.3mm x 6mm, (1)...

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·October 8, 2014

    REACH ACCESS DAILY FLOSSER

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON CONSUMER PRODUCTS·Product code JES·June 7, 2013

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011

    LIFE SCOPE G9

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·June 13, 2024

    LIFE SCOPE G9

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·October 27, 2023

    SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for radiation therapy treatments of malignant neoplastics diseases.

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·March 26, 2014