BEUDAMED
    1,465 results · 29ms · Sources: EU EUDAMED, US FDA

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    NovoFine 32G Tip (0.23/0.25) x 6 mm ETW (extra thin wall)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD¿ PEN NEEDLE STERILE SINGLE USE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMI·April 26, 2018

    23G ETW X 7MM PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMI·August 31, 2021

    23G ETW X 7MM PEN NEEDLE US

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMI·January 4, 2021

    MIRRAGEN ADVANCED WOUND MATRIX

    FDA Adverse Event
    Death ·ETW WOUIND CARE LLC·Product code FRO·August 14, 2018

    NOVOFINE 32G 6 MM

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S·Product code FMI·December 6, 2021

    23G ETW X 7MM PEN NEEDLE EU

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMI·November 14, 2018

    NOVOFINE 32G 6 MM

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S·Product code FMI·September 28, 2023

    NOVOFINE 8MM (30G) AUTOCOVER

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S, MS HJOERRING·Product code FMI·August 11, 2017

    NOVOFINE 32G 6 MM

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S·Product code FMI·December 22, 2023

    NOVOFINE 32G 6 MM

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S·Product code FMI·November 8, 2019

    NOVOFINE 32G 6 MM

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S·Product code FMI·August 16, 2023

    NOVOFINE 32G 6 MM

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S·Product code FMI·November 24, 2021

    BD 23G ETW X 7MM PEN NEEDLE¿ US

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMI·April 2, 2019

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 16, 2008

    ITREL II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 16, 2008

    ITREL II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 16, 2008

    ITREL II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 16, 2008

    ITREL II

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·September 16, 2008

    ITREL II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 16, 2008