BEUDAMED
    11 results · 28ms · 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.

    HYPER-HYPOTHERMIA UNIT HYPO 10-200

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INRATIO2 PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·March 30, 2016

    INRATIO2 PT/INR TEST STRIPS

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code GJS·March 30, 2016

    SYNTHES (USA) CALVICLE HOOK PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BAXTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code KPE·August 12, 2011

    INRATIO PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·October 18, 2016

    INRATIO PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·April 29, 2016

    CATH 5F INFINITI TL PIG145 110

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DQO·May 26, 2014

    PT HYBRID GLENOID POST REGENEREX POROUS TITANIUM CONSTRUCT

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code KWS·November 14, 2012

    LONG 45 ENDOCUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·September 12, 2007