BEUDAMED
    8 results · 19ms · 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 ×

    FAVC-HH: FEMORAL ARTERY VASCULAR CLAMP-HAND HELD: 1/2 & 3 POUNDS (RMDS810T/815T/820T)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THE GUIDER CORONARY GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BRAIN HEART INFUS AGAR SLANT W/10% SHEEP BLOOD C&C

    FDA 510(k)
    FDA Class 1 ·Microbiology

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·June 27, 2019

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    JUNCHENG·Product code ITJ·February 21, 2013

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·Product code NIM·January 28, 2011

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·August 1, 2014