Taiwan FDA registration 40a49a1b4833ccf00938eb1b258ae5e5
"Dirk" enterovirus antigen enzyme immunoassay group
TW: "德克" 腸病毒抗原酵素免疫試劑組
Taiwan·Risk Class 1·Baoling Fujin Biotechnology Co., Ltd. Medical Equipment Factory·Registered Nov 21, 2006 – Nov 21, 2011CancelledRegistration details
- Analysis ID
- 40a49a1b4833ccf00938eb1b258ae5e5
- Customs Code
- DHY04300171002
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Dirk International Limited
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Koshaki Virus Serum Reagent (C.3145)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3145 柯沙奇病毒血清試劑
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Nov 21, 2006
- Expiry Date
- Nov 21, 2011
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Dirk" enterovirus antigen enzyme immunoassay group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 40a49a1b4833ccf00938eb1b258ae5e5 and manufactured by Baoling Fujin Biotechnology Co., Ltd. Medical Equipment Factory. The authorized representative in Taiwan is Dirk International Limited.
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