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

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    CG FUTURE ANNULOPLASTY SYSTEM, MODEL 638R

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MOSAIC

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·March 12, 2019

    HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·May 27, 2020

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·June 11, 2021

    CG COMPOSITE RING

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·September 2, 2020

    DURAN ANCORE RING

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·September 2, 2020

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·May 16, 2023

    CG COMPOSITE RING

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·February 8, 2023

    Micro Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70611271·Micro Sprint-Brackets McLaugh/Benn/Trev. .022" ...

    ZAVATION

    FDA UDI
    Zavation LLC·00842166120174·PLIF-R Ti 11x27-14

    ZAVATION

    FDA UDI
    Zavation LLC·00842166120181·PLIF-R Ti 11x27-15

    ZAVATION

    FDA UDI
    Zavation LLC·00842166120167·PLIF-R Ti 11x27-13

    ZAVATION

    FDA UDI
    Zavation LLC·00842166120150·PLIF-R Ti 11x27-12

    ZAVATION

    FDA UDI
    Zavation LLC·00842166120198·PLIF-R Ti 11x27-16

    ORTHOPEDIC WIRE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ANCA COMBI DIAGNOSTIC KIT WITH IF-AIM TECHNOLOGY

    FDA 510(k)
    FDA Class 2 ·Immunology

    PROLENE POLYPROPYLENE SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAW·April 16, 2013

    UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·March 7, 2011

    MONACO

    FDA Adverse Event
    Malfunction ·COMPUTERIZED MEDICAL SYSTEMS, AN ELEKTA COMPANY·Product code MUJ·June 13, 2008

    NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026