Taiwan FDA registration 61b7b8772b07e4eaeac5bd9679b7e24f

"POWER WELL" Hernia support (Non-Sterile)

TW: "保衛" 疝脫支撐器 (未滅菌)

Taiwan·Risk Class 1·MD·POWER WELL HEALTHCARE TECHNOLOGY CO., LTD.·Registered Aug 08, 2017 – Aug 08, 2022Cancelled

Registration details

Analysis ID: 61b7b8772b07e4eaeac5bd9679b7e24f
License Form: Ministry of Health Medical Device Manufacturing No. 006868

Company information

Manufacturer: POWER WELL HEALTHCARE TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: POWER WELL HEALTHCARE TECHNOLOGY CO., LTD.

Product details

Product Type (Level 1): H Gastroenterology-urology devices
Product Type (Level 2): H5970 Hernia Brace
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 08, 2017
Expiry Date: Aug 08, 2022

Cancellation information

Status: Logged out
Reason: 轉為登錄字號

About this record

Access comprehensive regulatory information for "POWER WELL" Hernia support (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 61b7b8772b07e4eaeac5bd9679b7e24f and manufactured by POWER WELL HEALTHCARE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is POWER WELL HEALTHCARE TECHNOLOGY CO., LTD..

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