Taiwan FDA registration b4e9101bcaf07977c3044d3ea8016f75
Kaiwo Technology Follicular Mature Hormone Detection Kit
TW: 開物科技促濾泡成熟激素檢測試劑盒
Taiwan·Risk Class 1·SYNTRON BIORESEARCH INC.,·Registered Sep 26, 2007 – Sep 26, 2012CancelledRegistration details
- Analysis ID
- b4e9101bcaf07977c3044d3ea8016f75
- Customs Code
- DHA04400617404
Company information
- Manufacturer
- SYNTRON BIORESEARCH INC.,
- Manufacturer Country
- United States
- Authorized Representative
- Kaiwu Technology Co., Ltd. Tainan Branch
Product details
- Intended Use
- Limited to the first level identification scope of the follicle stimulating hormone test system (A.1300) of the medical device management measures.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1300 Follicular Stimulation Hormone Test System
- Import Information
- import
Dates and status
- Registration Date
- Sep 26, 2007
- Expiry Date
- Sep 26, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Kaiwo Technology Follicular Mature Hormone Detection Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b4e9101bcaf07977c3044d3ea8016f75 and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.
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