Taiwan FDA registration 7ad1d18011a453e557fba37242e1f1ca
Bioresearch Fast Neville Influenza Test Kit (Unsterilized)
TW: 生研快納威流行性感冒快速檢驗套組(未滅菌)
Taiwan·Risk Class 1·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered Aug 24, 2009 – Aug 24, 2024CancelledRegistration details
- Analysis ID
- 7ad1d18011a453e557fba37242e1f1ca
- Customs Code
- DHA04400797902
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3330 流感病毒血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Aug 24, 2009
- Expiry Date
- Aug 24, 2024
- Cancellation Date
- Jun 28, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Bioresearch Fast Neville Influenza Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7ad1d18011a453e557fba37242e1f1ca and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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