Taiwan FDA registration bf648cd61982daf7408dbffd0f869ce0

"Darco" hydrogel acne patch (unsterilized)

TW: “達可”水凝膠痘痘貼 (未滅菌)

Taiwan·Risk Class 1·Kaizhi Biotechnology Co., Ltd. Xinzhuang factory·Registered Jun 17, 2013 – Jun 17, 2018Cancelled

Registration details

Analysis ID: bf648cd61982daf7408dbffd0f869ce0

Company information

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

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;; Contract manufacturing

Dates and status

Registration Date: Jun 17, 2013
Expiry Date: Jun 17, 2018
Cancellation Date: Dec 05, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Darco" 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 bf648cd61982daf7408dbffd0f869ce0 and manufactured by Kaizhi Biotechnology Co., Ltd. Xinzhuang factory. The authorized representative in Taiwan is TACK BIOTECHNOLOGY CO., LTD..

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