Taiwan FDA registration d76504632b3790e08cff6972ed985ee4
"GHope" Influenza A&B Virus Antigen Rapid Test (Non-Sterile)
TW: "炬合" 流行性感冒病毒A型與B型快速檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·TAUNS LABORATORIES, INC.·Registered Jun 26, 2015 – Jun 26, 2020CancelledRegistration details
- Analysis ID
- d76504632b3790e08cff6972ed985ee4
- License Form
- Ministry of Health Medical Device Import No. 015386
- Customs Code
- DHA09401538600
Company information
- Manufacturer
- TAUNS LABORATORIES, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD.
Product details
- 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
- Jun 26, 2015
- Expiry Date
- Jun 26, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for "GHope" Influenza A&B Virus Antigen 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 d76504632b3790e08cff6972ed985ee4 and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..
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