Taiwan FDA registration a58fcefda4bb0ed8a520a3c089eeccae
Fukushima Rapid Prostate-Specific Antigen Assay Reagent
TW: 福島快取前列腺特異抗原快速測定試劑
Taiwan·Risk Class 2·VEDA LAB·Registered Apr 19, 2006 – Apr 19, 2011CancelledRegistration details
- Analysis ID
- a58fcefda4bb0ed8a520a3c089eeccae
- Customs Code
- DHA00601638503
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- Fukushima Medical Equipment Co., Ltd
Product details
- Intended Use
- Qualitative detection of prostate-specific antigen (PSA) 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 Rapid Prostate-Specific Antigen 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 a58fcefda4bb0ed8a520a3c089eeccae and manufactured by VEDA LAB. The authorized representative in Taiwan is Fukushima Medical Equipment Co., Ltd.
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