Taiwan FDA registration 95feff10b9b79abd00ba64fe81f28b15
"Seiken" Shamon bacteria antiserum
TW: 「生研」沙門氏菌抗血清
Taiwan·Risk Class 1·DENKA SEIKEN CO., LTD.·Registered May 05, 2006 – May 04, 2016CancelledRegistration details
- Analysis ID
- 95feff10b9b79abd00ba64fe81f28b15
- Customs Code
- DHA04400434903
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- LINKSEAS TRADING CO., LTD.
Product details
- Intended Use
- It is limited to the scope of first-level identification of medical equipment management measures [Salmonella serum reagent (C.3550)].
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3550 沙門氏菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- May 05, 2006
- Expiry Date
- May 04, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Seiken" Shamon bacteria antiserum in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 95feff10b9b79abd00ba64fe81f28b15 and manufactured by DENKA SEIKEN CO., LTD.. The authorized representative in Taiwan is LINKSEAS TRADING CO., LTD..
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