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 ×

    PLEASURE PLUS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PORTABLE X-RAY SYSTEM, MODEL HAND-RAY

    FDA 510(k)
    FDA Class 2 ·Dental

    ASCENT XXL CLOSED BOX FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMR HUMERAL HEAD Ø54 MM

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code KWT·November 12, 2019

    TRIAGE BNP TEST FOR BECKMAN COULTER

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code NBC·May 9, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

    BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code EOQ·November 18, 2010

    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

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021