BEUDAMED
    11 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 ×

    DENTAPURE DP 90 CARTRIDGE, DENTAPURE DP 365 CARTRIDGE

    FDA 510(k)
    FDA Class 1 ·Dental

    TYTAN AUTOMATIC ANEROID SPHYGMOMANOMETER, MODEL A730 AND MANUAL DIGITAL LCD SPHYGMOMANOMETER, MODEL A830 SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Straumann Ceramic Healing Abutments

    FDA 510(k)
    FDA Class 2 ·Dental

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATIA)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·June 7, 2006

    INRATIO PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·November 22, 2016

    NOTINGHM SHLDR HUM HEAD 48X17 OFFSET

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·January 19, 2016

    OPAL IMPL-HOLDER W/PISTOL GRIP

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·March 7, 2013

    TERUMO PERFUSION SYSTEM 8000

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code JOR·February 4, 2011

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·August 8, 2014