BEUDAMED
    7 results · 32ms · Sources: EU EUDAMED, US FDA

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    Total Hip Application (THA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is intended to assist the surgeon in providing software define spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures.

    FDA Recall
    Terminated ·Mako Surgical Corporation·Product code OLO·August 7, 2017

    Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is intended to assist the surgeon in providing software define spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures.

    FDA Recall
    Terminated ·Mako Surgical Corporation·Product code OLO·August 7, 2017

    Dunlee DA 200 Ultra & MX 200 Ultra CT X-Ray Tube Housing Assembly (989600088701); replacement x-ray tube housing assemblies; Dunlee, 555 North Commerce Street, Aurora, Illinois 60504 U.S.A.; part number 875-01

    FDA Recall
    Terminated ·Dunlee·Product code ITY·April 7, 2005

    Dunlee DA 200 PRO & MX 200 PRO CT X-Ray Tube Housing Assembly (989600088401); replacement x-ray tube housing assemblies; Dunlee, 555 North Commerce Street, Aurora, Illinois 60504 U.S.A.; part number 875-01

    FDA Recall
    Terminated ·Dunlee·Product code ITY·April 7, 2005

    Dunlee DA 200 & MX 200 CT X-Ray Tube Housing Assembly (989600087501); replacement x-ray tube housing assemblies; Dunlee, 555 North Commerce Street, Aurora, Illinois 60504 U.S.A.; part number 875-01

    FDA Recall
    Terminated ·Dunlee·Product code ITY·April 7, 2005

    Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.

    FDA Recall
    Terminated ·Teleflex Medical·Product code CCW·January 10, 2017

    Kits and Trays containing both alcohol swabstick/prep pad and lubricant: DeRoyal (R) AMNIOCENTESIS TRAY, LINK DREW LACO HOSP, REF 50-11656.02, Rx Only, STERILE EO, Manufactured by: DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849, USA.

    FDA Recall
    Terminated ·Deroyal Industries, Inc. Lafollette·Product code LRP·February 7, 2011