BEUDAMED
    9 results · 19ms · 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 ×

    BECKMAN COULTER FERRITIN REAGENT, MODEL: OSR61203

    FDA 510(k)
    FDA Class 2 ·Immunology

    MedStream

    FDA UDI
    MEDICAL SPECIALTIES DISTRIBUTORS, LLC·00842472106084·DRESSING CHANGE KIT

    SOPRO595 INTRA ORAL CAMERA

    FDA 510(k)
    FDA Class 1 ·Dental

    XIA SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    2520274-2013-02361

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·May 3, 2013

    OSCILL-SAW-ATTACHM F/532.001 532.010 532

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·September 16, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATIVE CENTER-SILICON VALLEY·Product code GEX·May 2, 2011

    The Maestro System 204-503, Straight Permucosal Ext, 5mm x 3mm

    FDA Recall
    Terminated ·BioHorizons Implant Systems Inc One Perimeter Park South·Product code NDP·June 3, 2005

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012