Taiwan FDA registration 5846541fdb748dbaa03a27b7488acccb
"GHope" Adenovirus Antigen Rapid Diagnostic Kit (Non-Sterile)
TW: "炬合" 腺病毒檢驗試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·TAUNS LABORATORIES, INC.·Registered Feb 25, 2014 – Feb 25, 2019CancelledRegistration details
- Analysis ID
- 5846541fdb748dbaa03a27b7488acccb
- License Form
- Ministry of Health Medical Device Import No. 013879
- Customs Code
- DHA09401387900
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)
- C3020 adenovirus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 25, 2014
- Expiry Date
- Feb 25, 2019
- 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" Adenovirus Antigen Rapid Diagnostic Kit (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 5846541fdb748dbaa03a27b7488acccb and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..
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