Taiwan FDA registration a4a25edbcd08b789f551521a36e97495
Fukushima Quick Fetch A Fetal Globulin Rapid Assay Reagent
TW: 福島快取甲型胎兒球蛋白快速測定試劑
Taiwan·Risk Class 2·VEDA LAB·Registered Apr 19, 2006 – Apr 19, 2011CancelledRegistration details
- Analysis ID
- a4a25edbcd08b789f551521a36e97495
- Customs Code
- DHA00601638605
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- Fukushima Medical Equipment Co., Ltd
Product details
- Intended Use
- Qualitative detection of alpha-fetal globulin in human whole blood, plasma, and 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
- Apr 19, 2006
- Expiry Date
- Apr 19, 2011
- Cancellation Date
- Nov 20, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Fukushima Quick Fetch A Fetal Globulin Rapid Assay Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a4a25edbcd08b789f551521a36e97495 and manufactured by VEDA LAB. The authorized representative in Taiwan is Fukushima Medical Equipment Co., Ltd.
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