Taiwan FDA registration 839eadd21b383aac1c9cd318f1932cc4
"Grace" Influenza A+B Influenza Virus Test Group (Unsterilized)
TW: "葛芮斯" A+B型流行性感冒病毒檢驗試驗組 (未滅菌)
Taiwan·Risk Class 1·CORIS BIOCONCEPT·Registered Jun 28, 2012 – Jun 28, 2017CancelledRegistration details
- Analysis ID
- 839eadd21b383aac1c9cd318f1932cc4
- Customs Code
- DHA04401189100
Company information
- Manufacturer
- CORIS BIOCONCEPT
- Manufacturer Country
- Belgium
- Authorized Representative
- APPLIED BIOTECH ENTERPRISE 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
- import
Dates and status
- Registration Date
- Jun 28, 2012
- Expiry Date
- Jun 28, 2017
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Grace" Influenza A+B Influenza Virus Test Group (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 839eadd21b383aac1c9cd318f1932cc4 and manufactured by CORIS BIOCONCEPT. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..
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