BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ADVIA 2120i, ADVIA 2120

    FDA 510(k)
    FDA Class 2 ·Hematology

    BI-METRIC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304254831·

    CRITIVIEW, MODEL CRV3

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    STEM: QUADRA-H CEMENTLESS, HA COATED STD SIZE 5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·February 21, 2020

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO·Product code LWS·October 10, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

    SYNCHRON LX® DILUENT I

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·July 15, 2011