BEUDAMED
    10 results · 27ms · 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 ×

    BIOPRO TARA FEMORAL RESURFACING COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BRECON KNITTING MILL, INC.

    FDA registration
    BRECON KNITTING MILL, INC.·1 product·🇺🇸 United States

    CHENG YI OPTICAL (XIAMEN) CO., LTD.

    FDA registration
    CHENG YI OPTICAL (XIAMEN) CO., LTD.·8 products·🇨🇳 China

    PREAMP CABLE, MODEL B400-1011PA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DENTIN CONDITIONING AND ADHESIVE SYSTEM (BOND-1)

    FDA 510(k)
    FDA Class 2 ·Dental

    POLYFLUX 17L

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - HECHINGEN BADEN DIALYZER·Product code KDI·January 14, 2020

    2520274-2013-01904

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·April 9, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·March 28, 2011

    ENDOTAK RELIANCE G

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

    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