BEUDAMED
    1,988 results · 22ms · Sources: EU EUDAMED, US FDA

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    SPpro GWI

    FDA UDI
    Neo Medical Inc.·B339SPG10127070·21ga x 7cm Sharps Safety Needle

    SPpro GWI

    FDA UDI
    Neo Medical Inc.·B339SPG10118070·18ga x 7cm Sharps Safety Needle

    SPpro GWI

    FDA UDI
    Neo Medical Inc.·B339SPG10119070·19ga x 7cm Sharps Safety Needle

    Guidewire Introducer Needle Square Hub Access Needle

    FDA UDI
    REMINGTON MEDICAL, INC.·00813079020349·19ga (1.1mm) x 7cm

    Guidewire Introducer Needle

    FDA UDI
    REMINGTON MEDICAL, INC.·00813079020301·18ga (1.3mm) x 7cm

    Guidewire Introducer Needle Square Hub Access Needle

    FDA UDI
    REMINGTON MEDICAL, INC.·00813079020325·18ga (1.3mm) x 7cm

    Guidewire Introducer Needle

    FDA UDI
    REMINGTON MEDICAL, INC.·00813079020332·19ga (1.1mm) x 7 cm

    MANAN GWI GUIDE WIRE INTRODUCERMANAN GWI GUIDE WIRE INTRODUCER

    FDA UDI
    Medical Components, Inc.·00884908028812·21GA X 7CM CLEAR HUB NEEDLE21GA

    MANAN GWI GUIDE WIRE INTRODUCERMANAN GWI GUIDE WIRE INTRODUCER

    FDA UDI
    Medical Components, Inc.·00884908029680·18GA X 7CM ONE-PART18GA X 7CM ON COURNAND NEEDL...

    MANAN GWI GUIDE WIRE INTRODUCERMANAN GWI GUIDE WIRE INTRODUCER

    FDA UDI
    Medical Components, Inc.·00884908028782·21GA X 4CM ECHO TIP21GA X 4CM EC NEEDLENEEDLE

    MANAN GWI GUIDE WIRE INTRODUCERMANAN GWI GUIDE WIRE INTRODUCER

    FDA UDI
    Medical Components, Inc.·00884908105285·22GA X 1.5" (3.8CM)22GA X 1.5" ( INTRODUCER NEE...

    CNS-6801A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·June 14, 2021

    MANAN GWI GUIDE WIRE INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MANAN GWI GUIDE WIRE INTRODUCER

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    Guidewire Introducer Needle Guidewire Access Needle

    FDA UDI
    REMINGTON MEDICAL, INC.·00813079021933·18ga (1.3mm) x 7cm

    Guidewire Introducer Needle Square Hub Access Needle

    FDA UDI
    REMINGTON MEDICAL, INC.·00813079021940·18ga (1.3mm) x 7cm

    BE PLUS LTM AMPLIFIER GWI AMPLIFIER

    FDA 510(k)
    FDA Class 2 ·Neurology

    EVIS LUCERA GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·March 16, 2026

    CNS-6801A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·June 14, 2021

    PRO SAFETY GWI NEEDLE

    FDA Adverse Event
    Malfunction ·NEO MEDICAL, INC.·Product code DWS·October 8, 2015