BEUDAMED
    22 results · 23ms · 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 Regulation: Us FDA ×

    Liver Access and Biopsy Sets

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·July 15, 2024

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·June 29, 2020

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·June 14, 2024

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·August 19, 2021

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·May 15, 2023

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·February 14, 2023

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·December 7, 2023

    LIVER ACCESS AND BIOPSY SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·January 27, 2022

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704294224·

    ANGLED TAPERED ABUTMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    PLAC TEST REAGENT KIT, MODELS 90107, 90112, 90115, 90116, 10-0112, 10-0113, 10-0115

    FDA 510(k)
    FDA Class 2 ·Immunology

    AESCULAP SURGICAL INSTRUMENTS

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

    AESCULAP SURGICAL INSTRUMENTS

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

    PAINSMART

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 23, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 15, 2014

    PROGAV SYS PED.W/SA 15 A.PRECHAMBER

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·April 4, 2019

    PROGAV 2.0 SYS PED.W/SA15 A.PRECHAMBER

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·August 6, 2020

    BIO-COMP SWVLK SP, 4.75X24.5MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MAI·September 16, 2019