Taiwan FDA registration ded7e69ae71af0f125021af06469e704

"Zhongli" suction regulator (unsterilized)

TW: "眾里"吸引調節器(未滅菌)

Taiwan·Risk Class 1·The second factory of Zhongli Technology Co., Ltd·Registered Sep 24, 2013 – Sep 24, 2028Active

Registration details

Analysis ID: ded7e69ae71af0f125021af06469e704

Company information

Manufacturer: The second factory of Zhongli Technology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: ACARE TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of the classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (J.6740)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6740 Vacuum-powered fluid absorption apparatus
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Sep 24, 2013
Expiry Date: Sep 24, 2028

About this record

Access comprehensive regulatory information for "Zhongli" suction regulator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ded7e69ae71af0f125021af06469e704 and manufactured by The second factory of Zhongli Technology Co., Ltd. The authorized representative in Taiwan is ACARE TECHNOLOGY CO., LTD..

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