BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    Cemented Origin Hip Stem

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Disposable Blade

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113196·BARD-PARKER BLADE #11 PACK OF 50

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112380·BARD-PARKER HANDLE #3

    LIGHT CURE RETAINER

    FDA 510(k)
    FDA Class 2 ·Dental

    PRIMED PLEATED TIE-BACK, PROCEDURE MASK PM4-305, PRIMED PLEATED EAR-LOOP, PROCEDURE MASK PM4-306

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    EON

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 17, 2014

    SUPREME EP CATHETER 5F, DECAPOLAR, CSL, 120 CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DRF·August 5, 2011

    INRATIO ASSY, BOX OF STRIPS, MULTILANGUAGE

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·June 27, 2013

    UNKNOWN EEA

    FDA Adverse Event
    Injury ·US SURGICAL PUERTO RICO·Product code GDW·March 22, 2019

    UNKNOWN EEA

    FDA Adverse Event
    Injury ·US SURGICAL PUERTO RICO·Product code GDW·March 22, 2019

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

    FDA Adverse Event
    Death ·HEARTWARE, INC.·Product code DSQ·January 16, 2020

    MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAN·August 10, 2021

    VICRYL PLUS POLYGLACTIN 910 SUTURE UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·August 10, 2021

    UNSPECIFIED BD EDTA TUBE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·January 15, 2020

    EXCOR BLOOD PUMP PU VALVES,25 ML IN/OUT Ø12 MM

    FDA Adverse Event
    Malfunction ·BERLIN HEART GMBH·Product code DSQ·May 2, 2019