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 ×

    TriClip Steerable Guide Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Life Spine SIMPACT Sacroiliac Joint Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Protect X Level 3 Isolation Gown

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    UNKNOWN ENDO GIA INSTRUMENT

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·November 21, 2008

    THERMOPHORE AUTOMATIC MOIST HEAT PACK

    FDA Adverse Event
    Malfunction ·BATTLE CREEK EQUIPMENT CO·Product code IRT·August 30, 2011

    GYNECARE TVT SECUR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code PAH·July 22, 2013

    SIRIUS HIP STEM 44-D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 24, 2019

    EXC ABT RNGLC-X SHELL PC 060MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 24, 2019