BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Malecot

    FDA UDI
    COOK INCORPORATED·00827002169227·Silicone Malecot Catheter

    ABSORBENT ANTIMICROBIAL WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    GRADIA DIRECT

    FDA 510(k)
    FDA Class 2 ·Dental

    DISTAL TARGETING DEVICE R1.5

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·February 22, 2012

    ADULT PUMP PACK

    FDA Adverse Event
    Malfunction ·ALLEGIANCE - SURGICAL GROUP·Product code KKX·January 3, 1997

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 29, 2013

    OPTISENSE

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 10, 2011

    VERTE-STACK SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·SOFAMOR DANEK DEGGENDORF GMBH·Product code MQP·July 25, 2008

    On-Board Imager - Exact Arm Elbow Motor Shaft (kVD, kVS, and MV) with ''Type 01" elbow motors. Product Usage: The On-Board Imager device is an x-ray device used for evaluation of correct patient position in relation to isocenter and verification of treatment fields in relation to anatomical and fiducial landmarks.

    FDA Enforcement
    Class II ·Terminated·Varian Medical Systems, Inc.·April 30, 2014

    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