Taiwan FDA registration dfc8684312fd536b646fb707550a252f
"Bioresearch" cholera and Vibrio enteritidis antiserum microbial reagents
TW: “生研”霍亂及腸炎弧菌抗血清微生物試劑
Taiwan·Risk Class 1·DENKA SEIKEN CO., LTD.·Registered Dec 06, 2006 – Dec 06, 2011CancelledRegistration details
- Analysis ID
- dfc8684312fd536b646fb707550a252f
- Customs Code
- DHA04400542103
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Hong Kong Commercial Mérieux S.p.A. Taiwan Branch
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Vibrio cholerae serum reagent (C.3930)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3930 霍亂弧菌血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 06, 2006
- Expiry Date
- Dec 06, 2011
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bioresearch" cholera and Vibrio enteritidis antiserum microbial reagents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfc8684312fd536b646fb707550a252f and manufactured by DENKA SEIKEN CO., LTD.. The authorized representative in Taiwan is Hong Kong Commercial Mérieux S.p.A. Taiwan Branch.
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