"Quanpeng" skin and mucous membrane wound cleanser (unsterilized) - Taiwan Registration 5785f26e0d4b7dde45aafd4bc1009e0c
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..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
Limited to the first level identification range of the "Liquid Bandage (J.5090)" Classification and Grading Management Measures for Medical Equipment.
J General hospital and personal use equipment
J.5090 Liquid bandages
Contract manufacturing;; Domestic
Dates and Status
Aug 28, 2019
Aug 28, 2029

