Taiwan FDA registration e1ce98a2ccc733252918a94753de7cfc
Vertical wide type B streptococcus reagent set (unsterilized)
TW: 立寬B型鏈球菌試劑組(未滅菌)
Taiwan·Risk Class 1·AMERITEK USA·Registered Jan 30, 2007 – Jan 30, 2022CancelledRegistration details
- Analysis ID
- e1ce98a2ccc733252918a94753de7cfc
- Customs Code
- DHA04600034402
Company information
- Manufacturer
- AMERITEK USA
- Manufacturer Country
- China
- Authorized Representative
- LIKWANG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3740 鏈球菌屬血清試劑
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 30, 2007
- Expiry Date
- Jan 30, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Vertical wide type B streptococcus reagent set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e1ce98a2ccc733252918a94753de7cfc and manufactured by AMERITEK USA. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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