BEUDAMED
    7 results · 31ms · 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 ×

    POLYMER COATED, POWDER-FREE LATEX EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SYNTHES (USA) 3.5 AND 4.5 MM LOCKING COMPRESSION PLATE SYSTEM WITH EXPANDED INDICATIONS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DULBECCO'S MODIFIED EAGLE'S MEDIUM NO. 200-2011

    FDA 510(k)
    FDA Class 1 ·Hematology

    XRL LARGE IMPLANT-INTEGRATED 29MM-37MM HEIGHT/0 DEG-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code MQP·August 4, 2017

    SYNCARDIA COMPANION 2 DRIVER

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, INC.·Product code LOZ·June 13, 2014

    INTERFACE 8252800 RESPONSE 2.0 INCREMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·February 25, 2013

    CONTOUR SE MICROSPHERES

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code HCG·February 9, 2011