BEUDAMED
    11 results · 20ms · 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 ×

    HSVI - IGG ELISA-KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704284966·JOHNSON NEUROMA RETRACTOR 5 1/2"

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704921079·

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209111282·

    SYDNEY IVF SPERM MEDIUM, SYDNEY IVF SPERM GRADIENT KIT, SYDNEY IVF SPERMIENT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    THE CRITERION II PACING SYS. MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EU 4.5X22MM STENT 12 MM DW TIP

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code NJE·June 24, 2021

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DTK·November 30, 2012

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·September 25, 2010

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015