BEUDAMED
    34 results · 27ms · Sources: EU EUDAMED, US FDA

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    POWERHEART AED G3 PRO

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496040637·LONG, SIZE M, MOKA, MICRO-MASSAGING LEGGINGS WI...

    CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    SONOTOME ULTRASONIC ASPIRATOR TIPS

    FDA 510(k)
    FDA Unclassified ·Unknown

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 11, 2012

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·March 23, 2022

    CADD MEDICATION CASSETTE

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·July 14, 2022

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTL, LTD.·Product code KWA·December 29, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 8, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 22, 2011

    STERLING OVER-THE-WIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·May 8, 2008

    CADD

    FDA Adverse Event
    Malfunction ·NULL·Product code FPA·August 17, 2021

    CADD MEDICATION CASSETTES

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

    NV EHXL ALIP LNR G2 36MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code OQI·September 25, 2023

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013

    ASR ACETABULAR CUPS 60

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·October 24, 2015

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 22, 2013

    ADAPTER SLEEVES 12/14 +8

    FDA Adverse Event
    Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·November 4, 2015

    ADAPTER SLEEVES

    FDA Adverse Event
    Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·February 2, 2016