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

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    Dyna-Vision Telemonitoring System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endo-Model Modular Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575340736·Femoral Segment,Size 3

    Endo-Model Modular Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575340729·Femoral Segment,Size 3

    Endo-Model Modular Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575340682·Femoral Segment,Size 3

    Endo-Model Modular Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575340712·Femoral Segment,Size 3

    Endo-Model Modular Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575340699·Femoral Segment,Size 3

    Endo-Model Modular Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575340675·Femoral Segment,Size 3

    IPUMP PAIN MANAGEMENT SYSTEM, MODEL 2L3107, 2L3107K

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SILVER DENTAL ARREST

    FDA 510(k)
    FDA Class 2 ·Dental

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 8, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 8, 2013

    ECLIPSE

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS FINLAND OY·Product code MUJ·June 28, 2011

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 2, 2021

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 9, 2019

    LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Right

    FDA Enforcement
    Class II ·Ongoing·Waldemar Link GmbH & Co. KG (Mfg Site)·July 5, 2023

    LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left

    FDA Enforcement
    Class II ·Ongoing·Waldemar Link GmbH & Co. KG (Mfg Site)·July 5, 2023

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 11, 2024

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 20, 2020

    SENRI

    FDA Adverse Event
    Injury ·KANEKA·Product code LIT·March 12, 2019