Taiwan FDA registration 5785f26e0d4b7dde45aafd4bc1009e0c

"Quanpeng" skin and mucous membrane wound cleanser (unsterilized)

TW: “全鵬”皮膚黏膜傷口清潔劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Zhudong Factory, Huanbo Technology Co., Ltd.; Quanpeng Technology Co., Ltd·Registered Aug 28, 2019 – Aug 28, 2029Active
Registration details
Analysis ID
5785f26e0d4b7dde45aafd4bc1009e0c
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
ATK ALLWAYS TECHNOLOGY CORP.
Product details
Intended Use
Limited to the first level identification range of the "Liquid Bandage (J.5090)" Classification and Grading Management Measures for Medical Equipment.
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5090 Liquid bandages
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Aug 28, 2019
Expiry Date
Aug 28, 2029
About this record

Access comprehensive regulatory information for "Quanpeng" skin and mucous membrane wound cleanser (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5785f26e0d4b7dde45aafd4bc1009e0c and manufactured by Zhudong Factory, Huanbo Technology Co., Ltd.; Quanpeng Technology Co., Ltd. The authorized representative in Taiwan is ATK ALLWAYS TECHNOLOGY CORP..

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