BEUDAMED
    8 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 ×

    HY-BOND POLYCARBOXYLATE CEMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    TrojanTM Azul Personal Lubricant (H2O Sensitive Touch Personal Lubricant)

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

    FILMARRAY RP PANEL

    FDA 510(k)
    FDA Class 2 ·Microbiology

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Injury ·AESCULAP INC·Product code KCT·October 12, 2016

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·GALWAY (RC) - RX·Product code CBK·March 21, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    BECKMAN COULTER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code CGA·August 16, 2010

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Malfunction ·AESCULAP INC·Product code KCT·July 26, 2016