BEUDAMED
    9,519 results · 48ms · Sources: EU EUDAMED, US FDA

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    Tapered Screw-Vent®

    FDA UDI
    ZimVie US Corp LLC·00889024014275·

    MORRISON MEDICAL

    FDA UDI
    MORRISON MEDICAL, LTD·00647921332119·PATHO RETRO 7' TWO PIECE

    TRI

    FDA UDI
    TRI Dental Implants Int. AG·07640149881639·

    AUTODELFIA NEONATAL 17A-OH-PROGESTERONE

    FDA Adverse Event
    Other ·WALLAC OY, PERKINELMER LAS·Product code JLX·March 6, 2009

    Automatic High-throughput Exosome Extractor

    FDA UDI
    Zhaorui Medical (Shenzhen) Co., LTD·06975064320002·

    SPECIMEN GATE SCREENING CENTER

    FDA Adverse Event
    Malfunction ·WALLAC OY, SUBSIDIARY OF PERKINELMER·Product code JQP·September 4, 2015

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code FMF·September 6, 2023

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·December 28, 2023

    ALARIS SYSTEM PUMP MODULE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH ALARIS PRODUCTS·Product code FRN·August 13, 2008

    SYRINGE, PISTON

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·January 17, 2024