BEUDAMED
    FDA Adverse Event Other Summary report: N

    CRANIAL PERFORATOR

    MDR report key: 21352 · Received April 3, 1995

    Report

    Report Number
    21352
    Event Type
    Other
    Date Received
    April 3, 1995
    Date of Event
    March 21, 1995
    Report Date
    March 24, 1995
    Manufacturer
    ACRA-CUT, INC.
    Product Code
    HBF
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    WHEN DRILLING CRANIAL BURR HOLE PERFORATOR DID NOT STOP PRIOR TO THE DURA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CRANIAL PERFORATOR CRANIAL PERFORATOR HBF ACRA-CUT, INC. 200-241 DRG-1 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Other