logobeta
본 영문본은 리걸엔진의 AI 번역 엔진으로 번역되었습니다. 수정이 필요한 부분이 있는 경우 피드백 부탁드립니다.
텍스트 조절
arrow
arrow
(영문) 수원지방법원 성남지원 2014.06.26 2014고정534
의료기기법위반
Text

Defendants shall be punished by a fine of KRW 300,000.

Defendant

If A does not pay the above fine, it shall be 100.

Reasons

Criminal facts

Defendant

A is a person who operates a D building in Seongbuk-gu, Sungnam-si, a corporation with Adong 2909, and Defendant B is a corporation that engages in import, sale, and manufacturing of medical devices.

1. No person shall put any indication on an outer package, packing material, or an accompanying document of any appliance other than a medical device, that is likely to mislead any person to believe that the appliance has a performance, efficacy, or effect similar to that of a medical device, or make any advertisement with the same content therein;

Nevertheless, from May 2012 to November 8, 2013, the Defendant sold “G” a breast-management movement machine, a product manufactured by F, company E and scood B, an Internet shopping business entity, through the Internet homepage B. “G” increased the blood by a conference vibration of 12,000 per minute 12,00, thereby making it effective for the improvement of the chest-friendly chest, scood, scood, scood, and so on. G’s home at the beginning of the end of the end of G is likely to have the effect of raising the utilization of the math and small scood scood scood, or raising the scood scood scood scood scood scood scood scood scood scood scood.

2. Defendant B, a representative of the Defendant, made an advertisement that could mislead Defendant A, as described in paragraph (1), to have performance, efficacy, and effect similar to that of a medical device.

Summary of Evidence

1. Defendants’ respective legal statements

1. Application of the Acts and subordinate statutes to the written accusation (including related materials);

1. Relevant Article of the Medical Devices Act and subparagraph A of the punishment: Defendant B shall be subject to a fine under each subparagraph of Article 52 (1) and each subparagraph of Article 26 (7) of the Medical Devices Act;

arrow