BEUDAMED
    16 results · 20ms · Sources: EU EUDAMED, US FDA

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    Merits P335 Powered Wheelchair

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MediBag

    FDA UDI
    SUMMIT MEDICAL PRODUCTS, INC.·00857595005831·MediBag-250 mL Dual Port (Needleless and Spike ...

    BD Universal Viral Transport

    FDA UDI
    COPAN ITALIA SPA·38053326009410·3 mL Vial, Flock Mini

    BD™ Universal Viral Transport Flock Mini

    FDA UDI
    BECTON, DICKINSON AND COMPANY·30382902205297·Kit Uvt 3Ml With Flocked Minitip

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707022565·CALIBRA BANDS 2ND MOLAR n.SUR 29

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180173163·5 MM Ø, 33 CM PROBE WITH "CM" MARKINGS

    BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·Product code FOZ·August 17, 2021

    Orion

    FDA 510(k)
    FDA Unclassified ·Unknown

    LARGE CENTRIFUGAL BLOOD PUMP, MODEL CP-2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNVIERSAL VIRAL TRANSPORT FOR VIRUSES, CHLAMYDIAE, MYCROPLASMAS, AND UREAPLASMAS

    FDA Adverse Event
    Malfunction ·BD·Product code JSM·November 22, 2024

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 21, 2014

    VALEO BALLOON EXAPNDABLE BILIARY STENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·July 18, 2011

    NUTRILINE TWINFLO NEONATAL PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH.·Product code LJS·August 6, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013

    BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·April 21, 2021

    Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset Used in combination with infusion pumps for continuous subcutaneous infusion of medication.

    FDA Enforcement
    Class II ·Terminated·Unomedical As·July 1, 2015