Taiwan FDA registration a0e339b72d3e7747676e9dc12d5c1623
Dairo Ovulation Rapid Test (Unsterilized)
TW: 戴洛 排卵快速檢測試劑 (未滅菌)
Taiwan·Risk Class 1·Equinox Biotech Co., Ltd·Registered Jun 20, 2016 – Jun 20, 2026ExpiredRegistration details
- Analysis ID
- a0e339b72d3e7747676e9dc12d5c1623
- Customs Code
- DHA09600274905
Company information
- Manufacturer
- Equinox Biotech Co., Ltd
- Manufacturer Country
- China
- Authorized Representative
- SUNGYIN BIO INTERNATIONAL CO., LTD.
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
- Input;; Chinese goods
Dates and status
- Registration Date
- Jun 20, 2016
- Expiry Date
- Jun 20, 2026
About this record
Access comprehensive regulatory information for Dairo Ovulation Rapid Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a0e339b72d3e7747676e9dc12d5c1623 and manufactured by Equinox Biotech Co., Ltd. The authorized representative in Taiwan is SUNGYIN BIO INTERNATIONAL CO., LTD..
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