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"Gaozhen" hernia release brace (unsterilized) - Taiwan Registration 35505840bc10a56695e73161bf2db2d1

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..

This page provides complete technical specifications, regulatory compliance details. 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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35505840bc10a56695e73161bf2db2d1
Registration Details
Taiwan FDA Registration: 35505840bc10a56695e73161bf2db2d1
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Device Details

"Gaozhen" hernia release brace (unsterilized)
TW: "้ซ˜็ฆŽ" ็–่„ซๆ”ฏๆ’ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

35505840bc10a56695e73161bf2db2d1

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of the hernia brace (H.5970) of the Measures for the Administration of Medical Devices.

H Gastroenterology and urology

H.5970 Hernia Removal Supporter

Domestic

Dates and Status

Feb 25, 2015

Feb 25, 2025

Sep 30, 2021

Cancellation Information

Logged out

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