BEUDAMED
    82 results · 27ms · Sources: EU EUDAMED, US FDA

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    DVT-2600

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Needle aspiration and injection

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113592·PERIBULBAR NEEDLE 25GA 16MM

    XLP - CPRotector® Deluxe - Orange Nylon Pouch

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588030067·XLP - CPRotector® Deluxe - Orange Nylon Pouch

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193113593·HA PEEK EVOS Straight, ,16mmx9mmx 22mm , FLAT ...

    PRO-FEMUR R

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NICORE MODEL NCP-1 EXTERNAL COUNTERPULSATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD PLASTIPAK¿ CONCENTRIC LUER LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 10, 2022

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·September 18, 2020

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·September 11, 2020

    ADMINISTRATION SET FOR HALO II AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·INFUTRONIX, LLC.·Product code FPA·August 19, 2022

    NIMBUS II PLUS AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·INFUTRONIX, LLC·Product code FRN·September 7, 2023

    ADMINISTRATION SET FOR HALO II AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·INFUTRONIX, LLC.·Product code FPA·September 19, 2022

    ADMINISTRATION SET FOR HALO II AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·INFUTRONIX, LLC.·Product code FPA·September 16, 2022

    ADMINISTRATION SET FOR HALO II AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·INFUTRONIX, LLC.·Product code FPA·September 16, 2022

    NIMBUS II PLUS AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·INFUTRONIX, LLC·Product code FRN·July 17, 2023

    NIMBUS II PLUS AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·INFUTRONIX, LLC·Product code FRN·September 7, 2023

    BD MAX SYSTEM, BD MAX INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code OOI·September 3, 2020

    ARTELON CMC SPACER

    FDA Adverse Event
    Injury ·ARTIMPLANT AB·Product code KYI·October 21, 2008

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 2, 2013