Taiwan FDA registration 29f5a01ac631b8d6cb83560de4959803

"Mighty" hernia release brace (unsterilized)

TW: "威亘"疝脫支撐器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Biaoshi Medical Technology Co., Ltd.;; Waigan Enterprises Limited·Registered Feb 19, 2020 – Feb 19, 2025Cancelled
Registration details
Analysis ID
29f5a01ac631b8d6cb83560de4959803
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
WELSHENG CORPORATION
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
Contract manufacturing;; Domestic
Dates and status
Registration Date
Feb 19, 2020
Expiry Date
Feb 19, 2025
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Mighty" 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 29f5a01ac631b8d6cb83560de4959803 and manufactured by Biaoshi Medical Technology Co., Ltd.;; Waigan Enterprises Limited. The authorized representative in Taiwan is WELSHENG CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Waigan Enterprises Limited;; The second plant of Biaoshi Medical Technology Co., Ltd, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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