Taiwan FDA registration 6e5bacd58991269910de43d8e4299d4f

"Qiancheng" scar patch (unsterilized)

TW: “芊城” 疤痕貼片(未滅菌)

Taiwan·Risk Class 1·Canlide Biotech Co., Ltd.;; Qiancheng Industrial Co., Ltd·Registered Aug 31, 2020 – Aug 31, 2025Expired

Registration details

Analysis ID: 6e5bacd58991269910de43d8e4299d4f

Company information

Manufacturer: Canlide Biotech Co., Ltd.;; Qiancheng Industrial Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: QIAN CHENG MEDICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Scar Treatment Silicone Products (I.4025)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4025 Silicone products for scar treatment
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Aug 31, 2020
Expiry Date: Aug 31, 2025

About this record

Access comprehensive regulatory information for "Qiancheng" scar 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 6e5bacd58991269910de43d8e4299d4f and manufactured by Canlide Biotech Co., Ltd.;; Qiancheng Industrial Co., Ltd. The authorized representative in Taiwan is QIAN CHENG MEDICAL CO., LTD..

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.