Taiwan FDA registration 61c63bed81effc6eb3732e58d3cde12b

Lux Hydrogel Acne Patch (Unsterilized)

TW: 樂適敷水凝膠痘痘貼(未滅菌)

Taiwan·Risk Class 1·Kaizhi Biotechnology Co., Ltd. Xinzhuang factory·Registered Apr 30, 2013 – Apr 30, 2018Cancelled

Registration details

Analysis ID: 61c63bed81effc6eb3732e58d3cde12b

Company information

Manufacturer: Kaizhi Biotechnology Co., Ltd. Xinzhuang factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Kaizhi Biotechnology Co., Ltd. Xinzhuang factory

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4018 親水性創傷覆蓋材
Import Information: Domestic

Dates and status

Registration Date: Apr 30, 2013
Expiry Date: Apr 30, 2018
Cancellation Date: May 16, 2016

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for Lux Hydrogel Acne Patch (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 61c63bed81effc6eb3732e58d3cde12b and manufactured by Kaizhi Biotechnology Co., Ltd. Xinzhuang factory. The authorized representative in Taiwan is Kaizhi Biotechnology Co., Ltd. Xinzhuang factory.

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