Events

radioactive therapy management system - Aria 의 안전성 경고

National Institute of Drugs and Food Surveillance (INVIMA)에 따르면, 해당 안전성 경고 는 Colombia 에서 manufacturer #121 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 사례 ID
    I1511-504
  • 사례 연번
    2014DM-0011561
  • 날짜
    2015-11-03
  • 사례 국가
    Colombia
  • 사례 출처
    INVIMA
  • 사례 출처 URL
    https://app.invima.gov.co/alertas/dispositivos-medicos-invima?page=168
  • 비고 / 경고
    Colombian data is current through June 2019. All of the data comes from the National Institute of Drugs and Food Surveillance (INVIMA), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Colombia.
  • 데이터 추가 비고

Device

radioactive therapy management system - Aria
  • 모델명 / 제조번호(시리얼번호)
    Software versions 10.X, 11.X, 13.0 and 13.5 with clinical evaluation license
  • 제품 설명
    The management of Aryan radio therapy is a series of software modules designed to handle the entire process of a patient's treatment course, which includes plans for treatment and handling of images allowing the authorized user to enter, access, modify, store and archive treatment data. administrative clinical images and storage. The information can be downloaded from the corporate system, diagnostic images, planning of treatments, simulation, verification and treatment. The management of radioactive Aryan therapy stores histories of treatment including the dose delivered in specific sites, providing the necessary tools to verify the treatments carried out. The management of Aryan radiotherapy is designed to help the oncology personnel in the management of the total course of patient treatment, approval of treatment plans, and execution of the quality assurance review of the treatment, that is, following up on the treatments applied and dosing applied to the specific site. Indications for use include any disease or condition treatable with radiation therapy, including but not limited to cancer, use of aria. Aria password: You need a username and password to start using aria. The system administrator creates a username and password in data administration (data management). Radiation therapy management ARIA DICOM RT DICOM RT is a DICOM interface that allows treatment plan data to be transferred between the external system (basically a treatment planning system) and the Aryan system. The data transfer interfaces are: ARIA LINK, DICOM, MULTI-VENDOR DICOM SERVIS (MVDS) ARIA DICOM printingThe DICOM PRINT printing system allows images to be sent to DICOM printers.Ary description • it is a new workspace that replaces the TAB of prescriptions in the RT box. The users can adapt to specific conditions all the attributes of their radiotherapeutic prescriptions including certain characteristics such as: prescription of multi-modality prescription of multi-energy multiple plans
  • Manufacturer
    manufacturer #121

Manufacturer

manufacturer #121
  • 제조사 모회사 (2017)
    Abbott Laboratories
  • 제조사 의견
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    NIDFSINVIMA