BEUDAMED
    2,533 results · 37ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    SPECIAL BOLUS NEEDLE HAI STRAIGHT LENGTH 1 3/8" (3.5CM)

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code PTI·May 14, 2026

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·September 12, 2025

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·April 13, 2026

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·October 22, 2025

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·October 24, 2025

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·December 12, 2025

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·August 13, 2025

    INTERA 3000

    FDA Adverse Event
    Injury ·INTERA ONCOLOGY·Product code LKK·October 2, 2023

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·April 29, 2026

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·December 12, 2025

    COBAS® LIAT® SARS-COV-2 & INFLUENZA A/B

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QLT·November 2, 2021

    COBAS® LIAT® SARS-COV-2 & INFLUENZA A/B

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QLT·November 2, 2021

    COBAS® LIAT® SARS-COV-2 & INFLUENZA A/B

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QLT·November 2, 2021

    COBAS® LIAT® SARS-COV-2 & INFLUENZA A/B

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QLT·November 2, 2021

    COBAS SARS-COV-2 & INFLUENZA A/B TEST FOR USE ON THE COBAS LIAT SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QJR·August 10, 2021

    INTERA 3000 HEPATIC ARTERY INFUSION PUMP OR PREP KIT

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code PTI·March 7, 2025

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·August 6, 2025

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY, INC·Product code LKK·October 25, 2024

    CODMAN PUMP AND CATHETER

    FDA Adverse Event
    Injury ·INTERA ONCOLOGY·Product code LKK·August 25, 2020

    MERSILENE POLYESTER FIBER SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·January 5, 2023