BEUDAMED
    8 results · 22ms · 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 ×

    TOTAL KNEE REPLACEMENT CEMENT KLASSIC TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·TOTAL JOINT ORTHOPEDICS, INC.·Product code JWH·August 18, 2020

    Klassic Knee System - Klassic Knee PS-Post Femur; Klassic Knee Tibial Insert, PS-Post, Std Poly; Klassic Knee Tibial Insert, PS-Post, E-Link Poly

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REEKROSS FAMILY OR OTW PTA CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WIRELESS/WIRED FDR D-EVO FLAT PANEL DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code GEI·March 4, 2015

    INSERTER F/TEN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·June 22, 2013

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 4, 2008

    UNICEL DXC 800 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JGS·July 8, 2011