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"Oulive" hernia release brace (unsterilized) - Taiwan Registration ad3b0f1f101773209f2d87bab58d7c7d

Access comprehensive regulatory information for "Oulive" 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 ad3b0f1f101773209f2d87bab58d7c7d and manufactured by The second factory of Biao Shi Medical Technology Co., Ltd. The authorized representative in Taiwan is OPPO MEDICAL CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Oper Co., Ltd.;; 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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ad3b0f1f101773209f2d87bab58d7c7d
Registration Details
Taiwan FDA Registration: ad3b0f1f101773209f2d87bab58d7c7d
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Device Details

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

Registration Details

ad3b0f1f101773209f2d87bab58d7c7d

Company Information

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;; Contract manufacturing

Dates and Status

Oct 05, 2016

Oct 05, 2026

Sep 30, 2021

Cancellation Information

Logged out

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