Taiwan FDA registration ff928883846cb21d3befb6e8b4d2534b

"Keyun" alginate dressing (sterilization)

TW: “科云”藻酸鈣敷料 (滅菌)

Taiwan·Risk Class 1·Keyun Biomedical Technology Co., Ltd·Registered Sep 30, 2011 – Sep 30, 2021Cancelled

Registration details

Analysis ID: ff928883846cb21d3befb6e8b4d2534b

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: 國產;; QMS/QSD

Dates and status

Registration Date: Sep 30, 2011
Expiry Date: Sep 30, 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 "Keyun" alginate dressing (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ff928883846cb21d3befb6e8b4d2534b and manufactured by Keyun Biomedical Technology Co., Ltd. The authorized representative in Taiwan is Keyun Biomedical Technology Co., Ltd.

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