BEUDAMED
    36 results · 23ms · Sources: EU EUDAMED, US FDA

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    CHEETAH RELIANT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113998·HYDRO-DISSECT CANNULA VERTICAL 27GA

    PMT CORPORATION - STEREOTACTIC

    FDA UDI
    PMT CORPORATION·00650551149354·BRW/CRW STERILIZATION TRAY FOR SEEG 2.4MM DRILL...

    SONTEC WIRE PASSER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896051973·SONTEC WIRE PASSER SINGLE ENDED TIP PHENOLIC HA...

    I-LIPO, MODELS A00-1238 (230V), A00-1239 (120V)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    4D-VIEW 9.1 (4D VIEW PC SOFTWARE) MODEL: H48651SZ

    FDA 510(k)
    FDA Class 2 ·Radiology

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·July 23, 2021

    GALAXY G3 MINI 1MM X 4CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·June 19, 2020

    UNKNOWN - M2A-38 CUP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 9, 2013

    PROWLER SELECT MICROCATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code KRA·September 19, 2014

    CAPSUREFIX

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·May 25, 2011

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 12, 2021

    GALAXY G3 MINI 1MM X 4CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·October 1, 2022

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 6, 2021

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 6, 2021

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 12, 2021

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 6, 2021

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 6, 2021

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 6, 2021

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 6, 2021