Taiwan FDA registration 6b1bf3c6056e2d5ae1bc68b4c283e8ce
OPPO Medical Hernia support (Non-Sterile)
TW: 歐活 疝脫支撐器 (未滅菌)
Taiwan·Risk Class 1·MD·The second factory of Biao Shi Medical Technology Co., Ltd·Registered Feb 19, 2022 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- 6b1bf3c6056e2d5ae1bc68b4c283e8ce
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. a00106
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- The second factory of Biao Shi Medical Technology Co., Ltd
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)
- H5970 Hernia Brace
Dates and status
- Registration Date
- Feb 19, 2022
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for OPPO Medical Hernia support (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6b1bf3c6056e2d5ae1bc68b4c283e8ce and manufactured by The second factory of Biao Shi Medical Technology Co., Ltd. The authorized representative in Taiwan is The second factory of Biao Shi Medical Technology Co., Ltd.
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