Taiwan FDA registration eb8d6dadac71bcbcfdbff01f98baac66
Genisis influenza virus test reagent type A+B
TW: 吉尼西斯A+B型流行性感冒病毒檢驗試劑
Taiwan·Risk Class 1·HANGZHOU GENESIS BIODETECTION & BIOCONTROL CO., LTD·Registered Aug 02, 2010 – Aug 02, 2015CancelledRegistration details
- Analysis ID
- eb8d6dadac71bcbcfdbff01f98baac66
- Customs Code
- DHA04600100001
Company information
- Manufacturer Country
- China
- Authorized Representative
- LIKWANG INSTRUMENTS CO., LTD.
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
- Chinese goods;; input
Dates and status
- Registration Date
- Aug 02, 2010
- Expiry Date
- Aug 02, 2015
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Genisis influenza virus test reagent type A+B in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eb8d6dadac71bcbcfdbff01f98baac66 and manufactured by HANGZHOU GENESIS BIODETECTION & BIOCONTROL CO., LTD. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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