Taiwan FDA registration de0c6a13a8997e210161ed5c88d0a2af
"healgen" influenza A&B rapid test (Non-Sterile)
TW: "基因" A/B 型流感快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY·Registered Mar 14, 2016 – Mar 14, 2021ExpiredRegistration details
- Analysis ID
- de0c6a13a8997e210161ed5c88d0a2af
- License Form
- Ministry of Health Medical Device Import No. 016255
- Customs Code
- DHA09401625503
Company information
- Manufacturer
- HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- MIN JIER FIRM
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 devices
- Product Type (Level 2)
- C3330 Influenza virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 14, 2016
- Expiry Date
- Mar 14, 2021
About this record
Access comprehensive regulatory information for "healgen" influenza A&B rapid test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number de0c6a13a8997e210161ed5c88d0a2af and manufactured by HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY. The authorized representative in Taiwan is MIN JIER FIRM.
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