Taiwan FDA registration a5f05df52d40ca88389634c1efc9fd72

VENEX waterproof and breathable protective film (unsterilized)

TW: 維尼適防水透氣保護膜 (未滅菌)

Taiwan·Risk Class 1·Kaizhi Biotechnology Co., Ltd. Xinzhuang factory·Registered Oct 01, 2013 – Oct 01, 2018Cancelled

Registration details

Analysis ID: a5f05df52d40ca88389634c1efc9fd72

Company information

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

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Wound/Burn Dressings for Closure (I.4020)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4020 閉合用傷口/燒燙傷敷料
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Oct 01, 2013
Expiry Date: Oct 01, 2018
Cancellation Date: Jun 22, 2022

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for VENEX waterproof and breathable protective film (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a5f05df52d40ca88389634c1efc9fd72 and manufactured by Kaizhi Biotechnology Co., Ltd. Xinzhuang factory. The authorized representative in Taiwan is LINLI CO., LTD..

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