Taiwan FDA registration a13e6cc8e8573981e1b767e72b67f57b

"Oulive" hernia release brace (unsterilized)

TW: "歐活" 疝脫支撐器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Oper Co., Ltd.;; The second plant of Biaoshi Medical Technology Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
a13e6cc8e8573981e1b767e72b67f57b
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
OPPO MEDICAL CORP.
Product details
Intended Use
Limited to the classification and grading management measures of medical equipment "Hernia supporter (H.5970) first level identification range".
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.5970 Hernia Removal Supporter
Import Information
Domestic;; Contract manufacturing
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

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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