Taiwan FDA registration 514611e2825f4e2747f742279809f6ed
Fukushima Kotake pylori rapid assay reagent
TW: 福島快取幽門桿菌快速測定試劑
Taiwan·Risk Class 1·VEDA LAB·Registered Dec 22, 2005 – Dec 22, 2010CancelledRegistration details
- Analysis ID
- 514611e2825f4e2747f742279809f6ed
- Customs Code
- DHA04400230400
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- Fukushima Medical Equipment Co., Ltd
Product details
- Intended Use
- Qualitative detection of Helicobacter pylori IgG antibodies in human whole blood, plasma, and serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.0003 螺旋桿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 22, 2005
- Expiry Date
- Dec 22, 2010
- 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 Kotake pylori rapid assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 514611e2825f4e2747f742279809f6ed and manufactured by VEDA LAB. The authorized representative in Taiwan is Fukushima Medical Equipment Co., Ltd.
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