BEUDAMED
    831 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 ×

    UNIVERSAL COUCHTOP RECTANGULAR EXTENSION

    FDA Adverse Event
    Other ·MEDTEC, INC.·Product code IXQ·June 11, 2010

    DIAGNOST 76 PLUS

    FDA Adverse Event
    Malfunction ·PHILIPS SYSTEME MEDEZIN·Product code IXQ·September 15, 1997

    SERIES 8000 BUCKY

    FDA Adverse Event
    Injury ·LIEBEL FLARSHEIM·Product code IXQ·June 3, 1993

    *

    FDA Adverse Event
    CARESTREAM HEALTH, INC.·Product code IXQ·August 19, 2014

    IBEAM

    FDA Adverse Event
    Other ·MEDICAL INTELLIGENCE MEDIZINTECHNIK-GMBH·Product code IXQ·August 5, 2011

    DEL EV200 TABLE

    FDA Adverse Event
    Injury ·DEL MEDICAL GROUP·Product code IXQ·June 29, 2003

    SUMMIT INDUSTRIES LLC

    FDA Adverse Event
    Malfunction ·SUMMIT INDUSTRIES LLC.·Product code IXQ·June 8, 2016

    SBRT

    FDA Adverse Event
    Death ·Product code IXQ·February 13, 2015

    BK-200

    FDA Adverse Event
    Malfunction ·SHIMADZU COPORATION·Product code IXQ·March 23, 2018

    CONNEXION IMAGING MODULE

    FDA Adverse Event
    Malfunction ·MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH·Product code IXQ·April 10, 2018

    CIVCO Type-S Extension, REF MTIL6605, Reusable non-sterile extension for use with Universal Couchtop. The firm name on the label is CIVCO, Orange City, IA. For use to support and aid in positioning a patient during radiologic and other medical procedures.

    FDA Recall
    Terminated ·Med Tec Inc·Product code IXQ·June 21, 2010

    CIVCO SBRT System, REF MTSBRT001, containing CIVCO Pro-Lok Platform, REF MTSBRT002. Firm name on label is CIVCO, Orange City, Iowa Product Usage: The recalled product is intended to support and aid in positioning a patient during radiologic and other medical procedures.

    FDA Recall
    Terminated ·Civco Medical Instruments Inc·Product code IXQ·December 30, 2010

    CIVCO SBRT System, REF MTSBRT001L, containing CIVCO Pro-Lok Platform, REF MTSBRT002. Firm name on label is CIVCO, Orange City, Iowa Product Usage: The recalled product is intended to support and aid in positioning a patient during radiologic and other medical procedures.

    FDA Recall
    Terminated ·Civco Medical Instruments Inc·Product code IXQ·December 30, 2010

    CIVCO Rectangular Extension, REF MTIL6600, Reusable non-sterile extension for use with Universal Couchtop. The firm name on the label is CIVCO, Orange City, IA. For use to support and aid in positioning a patient during radiologic and other medical procedures.

    FDA Recall
    Terminated ·Med Tec Inc·Product code IXQ·June 21, 2010

    CIVCO Posifix Extension, REF MTIL6606, Reusable non-sterile extension for use with the Universal Couchtop. The firm name on the label is CIVCO, Orange City, IA. For use to support and aid in positioning a patient during radiologic and other medical procedures.

    FDA Recall
    Terminated ·Med Tec Inc·Product code IXQ·June 21, 2010

    Foot Lok Cusion, Part Number MTAFS01, reusable nonsterile (20.3 x 42 x 25.4cm) cushion.

    FDA Recall
    Terminated ·Med Tec Inc·Product code IXQ·March 6, 2009

    CIVCO Pro-Lok Platform, REF MTSBRT002. Firm name on label is CIVCO, Orange City, Iowa Product Usage: The recalled product is intended to support and aid in positioning a patient during radiologic and other medical procedures.

    FDA Recall
    Terminated ·Civco Medical Instruments Inc·Product code IXQ·December 30, 2010

    Table, Radiographic, Stationary Top

    FDA classification
    FDA Class 2 ·Table, Radiographic, Stationary Top

    MEGA ISQ

    FDA 510(k)
    FDA Class 1 ·Dental

    Sculpt I.Q.

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D74666592001·EasyBend - Bending tool