Taiwan FDA registration 7ad746af621aae8a1d7cf483950c37cf

"Shinyun" hydrophilic wound bedding (sterilization)

TW: “科云”親水性傷口敷料 (滅菌)

Taiwan·Risk Class 1·Keyun Biomedical Technology Co., Ltd·Registered Nov 16, 2011 – Nov 16, 2021Cancelled

Registration details

Analysis ID: 7ad746af621aae8a1d7cf483950c37cf

Company information

Manufacturer: Keyun Biomedical Technology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Keyun Biomedical Technology 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: QMS/QSD;; 國產

Dates and status

Registration Date: Nov 16, 2011
Expiry Date: Nov 16, 2021
Cancellation Date: Oct 12, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Shinyun" hydrophilic wound bedding (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7ad746af621aae8a1d7cf483950c37cf and manufactured by Keyun Biomedical Technology Co., Ltd. The authorized representative in Taiwan is Keyun Biomedical Technology Co., Ltd.

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