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

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    Lung Vision

    FDA 510(k)
    FDA Class 2 ·Radiology

    Biomet® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868308871·

    BIOMET HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304256262·

    ORION II CT CVC

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FINECUBE DENTAL CT

    FDA 510(k)
    FDA Class 2 ·Radiology

    CADD MEDICATION CASSETTE RESERVOIRS WITH FLOW STOP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·March 15, 2022

    CADD MEDICATION CASSETTE

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·April 6, 2022

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·October 10, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 11, 2013

    SLEEK OTW

    FDA Adverse Event
    Other ·CLEARSTREAM TECHNOLOGIES, LTD.·Product code LIT·June 8, 2011

    BD MICROTAINER® SST¿ TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·June 7, 2018

    26MM DIA COCR MOD HD STD NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2015

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026