Taiwan FDA registration 08ade3e6677fc10cfb23e10ed0fd75f3
Mitsubishi α-fetal protein test reagent
TW: 三菱α-胎兒蛋白檢驗試劑
Taiwan·MITSUBISHI KAGAKU IATRON. INC.·Registered Jul 14, 2006 – Jul 14, 2011CancelledRegistration details
- Analysis ID
- 08ade3e6677fc10cfb23e10ed0fd75f3
- Customs Code
- DHA00601722104
Company information
- Manufacturer
- MITSUBISHI KAGAKU IATRON. INC.
- Manufacturer Country
- Japan
- Authorized Representative
- Jingxiang Co., Ltd
Product details
- Intended Use
- To measure the intensity of AFP in human serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.6010 腫瘤相關抗原免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jul 14, 2006
- Expiry Date
- Jul 14, 2011
- Cancellation Date
- Oct 30, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Mitsubishi α-fetal protein test reagent in Taiwan's medical device market through Pure Global AI's free database. is registered under number 08ade3e6677fc10cfb23e10ed0fd75f3 and manufactured by MITSUBISHI KAGAKU IATRON. INC.. The authorized representative in Taiwan is Jingxiang Co., Ltd.
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