Taiwan FDA registration 1d1612f5c6b6f7728fc0bacad3db9ff5

“Acare”Pulse Oximeter

TW: “眾里”血氧濃度計

Taiwan·Risk Class 2·MD·The second factory of Zhongli Technology Co., Ltd·Registered May 31, 2022 – May 31, 2027Active

Registration details

Analysis ID: 1d1612f5c6b6f7728fc0bacad3db9ff5
License Form: Ministry of Health Medical Device Manufacturing No. 007477

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: Details are as detailed as approved Chinese instructions
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E2700 Oximeter
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 31, 2022
Expiry Date: May 31, 2027

About this record

Access comprehensive regulatory information for “Acare”Pulse Oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d1612f5c6b6f7728fc0bacad3db9ff5 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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