Taiwan FDA registration dc67325079b38a63583e8fdc13e9c323
"Bioken" Shigella antiserum reagent (unsterilized)
TW: "生研" 志賀氏菌抗血清試劑 (未滅菌)
Taiwan·Risk Class 1·DENKA CO., LTD·Registered Jul 12, 2010 – Jul 12, 2025ExpiredRegistration details
- Analysis ID
- dc67325079b38a63583e8fdc13e9c323
- Customs Code
- DHA04400898308
Company information
- Manufacturer
- DENKA CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- It is limited to the first-level identification scope of Shigella serum reagent (C.3660) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3660 志賀氏桿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Jul 12, 2010
- Expiry Date
- Jul 12, 2025
About this record
Access comprehensive regulatory information for "Bioken" Shigella antiserum reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dc67325079b38a63583e8fdc13e9c323 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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