Taiwan FDA registration a975e91d28710c6f942826c44c890e0c
OPPO Medical Cold/Hot Pack (Non-Sterile)
TW: 歐活 冷熱敷包 (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
- a975e91d28710c6f942826c44c890e0c
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. a00108
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 of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (O.5700)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O5700 Hot and cold compress device for medical use
Dates and status
- Registration Date
- Feb 19, 2022
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for OPPO Medical Cold/Hot Pack (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 a975e91d28710c6f942826c44c890e0c 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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