Taiwan FDA registration ad3b0f1f101773209f2d87bab58d7c7d

"Oulive" hernia release brace (unsterilized)

TW: "歐活" 疝脫支撐器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·The second factory of Biao Shi Medical Technology Co., Ltd·Registered Oct 05, 2016 – Oct 05, 2026Cancelled
Registration details
Analysis ID
ad3b0f1f101773209f2d87bab58d7c7d
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
OPPO MEDICAL CORP.
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
Domestic;; Contract manufacturing
Dates and status
Registration Date
Oct 05, 2016
Expiry Date
Oct 05, 2026
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 "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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