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"Oulive" hernia release brace (unsterilized) - Taiwan Registration a13e6cc8e8573981e1b767e72b67f57b

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 a13e6cc8e8573981e1b767e72b67f57b and manufactured by Oper Co., Ltd.;; The second plant of Biaoshi 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 The second factory of Biao Shi 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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a13e6cc8e8573981e1b767e72b67f57b
Registration Details
Taiwan FDA Registration: a13e6cc8e8573981e1b767e72b67f57b
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Device Details

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

Registration Details

a13e6cc8e8573981e1b767e72b67f57b

Company Information

Product Details

Limited to the classification and grading management measures of medical equipment "Hernia supporter (H.5970) first level identification range".

H Gastroenterology and urology

H.5970 Hernia Removal Supporter

Domestic;; Contract manufacturing

Dates and Status

Oct 01, 2021

Oct 31, 2026

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