Taiwan FDA registration 32fdbd77e6eb88562ef6ed6ce8abfa0d
"Zhongli" household treatment humidifier (unsterilized)
TW: “眾里”家用治療潮濕器 (未滅菌)
Taiwan·Risk Class 1·The second factory of Zhongli Technology Co., Ltd·Registered Jul 21, 2011 – Jul 21, 2026ExpiredRegistration details
- Analysis ID
- 32fdbd77e6eb88562ef6ed6ce8abfa0d
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ACARE TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Household Treatment Moisturizer (D.5460)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5460 家用治療潮濕器
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 21, 2011
- Expiry Date
- Jul 21, 2026
About this record
Access comprehensive regulatory information for "Zhongli" household treatment humidifier (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 32fdbd77e6eb88562ef6ed6ce8abfa0d 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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