BEUDAMED
    14 results · 36ms · Sources: EU EUDAMED, US FDA

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    LMA Fastrach ETT SU

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BENCO

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975004048·XX-Fine-/X-Coarse Assorted Benco Dental Absorbe...

    SIRION Lateral Lumbar Interbody Fusion

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CUMULASE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·November 11, 2014

    ACCU-CHEK ® SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS, INC.·Product code LZG·July 23, 2013

    VALVE CONTEGRA

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code MWH·February 1, 2019

    MELODY TRANSCATHETER PULMONARY VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPV·February 1, 2019

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·February 1, 2019

    HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·February 1, 2019

    FREESTYLE AORTIC ROOT BIOPROSTHESIS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·February 1, 2019

    TMC SPEEDMTP

    FDA Adverse Event
    Injury ·TREACE MEDICAL CONCEPTS, INC.·Product code JDR·April 1, 2025

    Factor VIII Chromogenic Assay, REF/Catalog No. B4238-40, Siemens Material Number (SMN) 10445729, IVD. --- CLASSIFICATION NAME: Test, Qualitative and Quantitative Factor Deficiency

    FDA Recall
    Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code GGP·November 19, 2015