Taiwan FDA registration a030992db9e84a3a3af31bb900273ccd
Medical Aesthetic Portable Ovulation Test Recorder (Unsterilized)
TW: 醫試美 攜帶式排卵偵測紀錄器 (未滅菌)
Taiwan·Risk Class 1·Kaiwu Technology Co., Ltd. Nanke Factory·Registered Feb 15, 2017 – Feb 15, 2027ActiveRegistration details
- Analysis ID
- a030992db9e84a3a3af31bb900273ccd
Company information
- Manufacturer
- Kaiwu Technology Co., Ltd. Nanke Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Kaiwu Technology Co., Ltd. Nanke Factory
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Luteinizing hormone test system (A.1485)" first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Feb 15, 2017
- Expiry Date
- Feb 15, 2027
About this record
Access comprehensive regulatory information for Medical Aesthetic Portable Ovulation Test Recorder (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a030992db9e84a3a3af31bb900273ccd and manufactured by Kaiwu Technology Co., Ltd. Nanke Factory. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Nanke Factory.
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