(1) Photographing stand with motorized lifting step AS - MK 4 (2) Wall mounting photographing stand AS - MK 5 (3) Standing photographing stand AS - MK 6 의 리콜
Pharmaceuticals and Medical Devices Agency, Japan에 따르면, 해당 리콜 는
Japan
에서 Auto system 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.
Japanese data is current through August 2018. All of the data comes from the Japanese Pharmaceuticals and Medical Devices Agency, 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 Japan.
(1) Electric patient table for general-purpose X-ray diagnostic apparatus (2) Non-motorized patient table for general-purpose X-ray diagnostic apparatus (3) Electric patient table for general purpose X-