Events

Magnetic Resonance Computerized Tomography System, Superconducting Magnetic Resonance Magnetic Resonance Computerized Tomography System, Superconducting Magnetized Magnetic Resonance Computerized Tomography System, Superconducting Magnetized Magnetic Resonance Computed Tomography System, Superconducting Magnetized Magnetic Resonance Computerized Magnetic Resonance System, Superconducting Magnetized Magnetic System Magnetic Resonance Computerized Tomography System, Superconducting Magnetic Resonance Magnetic Resonance Computerized Tomography System, Superconducting Magnetized Magnetic Resonance Computerized Tomography System, Superconducting Magnetized Magnetic Resonance Computed Tomography System, Superconducting Magnetized Magnetic Resonance Computerized Magnetic Resonance System, Superconducting Magnetized Magnetic System Magnetic Resonance Computed Tomography System, Superconducting Magnetic Resonance Magnetic Resonance Computed Tomography System, Superconducting Magnetic Resonance Magnetic Resonance Computed Tomography System, Magnetic Resonance Computed Tomography System, Superconducting Magnetized Magnetic Resonance Computerized Magnetic Resonance Computed Tomography System, Magnetic Resonance Computed Tomography System , Magnetic ball Magnetic Resonance Computed Tomography System, Magnetic Resonance Computed Tomography System, Magnetic Resonance Computed Tomography System 의 리콜

Korean Food & Drug Administration에 따르면, 해당 리콜 는 South Korea 에서 Ji Health Care Korea Co., Ltd. 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    250
  • 날짜
    2015-01-20
  • 사례 국가
    South Korea
  • 사례 출처
    KFDA
  • 사례 출처 URL
    https://emed.mfds.go.kr
  • 비고 / 경고
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, 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 South Korea.
  • 데이터 추가 비고
    The Korean Society of Food Science and Nutrition 09-292, 09-292, 09-292, 09-292, 09-292, No. 407, No. 10-820, No. 10-945, No. 10-946, No. 12-599, No. 98-52, No. 98-53, No. 99-3292, No. 99-2954 No. 02-374, No. 98-1457

Device

Magnetic Resonance Computerized Tomography System, Superconducting Magnetic Resonance Magnetic Re...

Manufacturer

Ji Health Care Korea Co., Ltd.