Taiwan FDA registration d78d0a7dc13f57df2ec4ee65fa8f4708

BIUS Hernia Removal Brace (Unsterilized)

TW: 彪仕疝脫支撐器 (未滅菌)

Taiwan·Risk Class 1·The second factory of Biao Shi Medical Technology Co., Ltd·Registered May 11, 2023 – Oct 31, 2025Expired

Registration details

Analysis ID: d78d0a7dc13f57df2ec4ee65fa8f4708

Company information

Manufacturer: The second factory of Biao Shi Medical Technology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PLUS MEDITECH CO., LTD.

Product details

Intended Use: Limited to the classification and grading management measures of medical equipment "Hernia supporter (H.5970) first level identification range".
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.5970 Hernia Removal Supporter

Dates and status

Registration Date: May 11, 2023
Expiry Date: Oct 31, 2025

About this record

Access comprehensive regulatory information for BIUS Hernia Removal 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 d78d0a7dc13f57df2ec4ee65fa8f4708 and manufactured by The second factory of Biao Shi Medical Technology Co., Ltd. The authorized representative in Taiwan is PLUS MEDITECH CO., LTD..

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