Taiwan FDA registration 35505840bc10a56695e73161bf2db2d1

"Gaozhen" hernia release brace (unsterilized)

TW: "高禎" 疝脫支撐器 (未滅菌)

Taiwan·Risk Class 1·KAO CHEN ENTERPRISE CO., LTD.·Registered Feb 25, 2015 – Feb 25, 2025Cancelled

Registration details

Analysis ID: 35505840bc10a56695e73161bf2db2d1

Company information

Manufacturer: KAO CHEN ENTERPRISE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: KAO CHEN ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of the hernia brace (H.5970) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.5970 Hernia Removal Supporter
Import Information: Domestic

Dates and status

Registration Date: Feb 25, 2015
Expiry Date: Feb 25, 2025
Cancellation Date: Sep 30, 2021

Cancellation information

Status: Logged out
Reason: 轉為登錄字號

About this record

Access comprehensive regulatory information for "Gaozhen" hernia release brace (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 35505840bc10a56695e73161bf2db2d1 and manufactured by KAO CHEN ENTERPRISE CO., LTD.. The authorized representative in Taiwan is KAO CHEN ENTERPRISE CO., LTD..

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