Taiwan FDA registration 15e52024162e09a6711fbef466190f36
"GHope" Respiratory Syncytial Virus (RSV) Rapid Test (Non-sterile)
TW: "炬合" 呼吸道融合細胞病毒快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·TAUNS LABORATORIES, INC.·Registered Sep 17, 2015 – Sep 17, 2020CancelledRegistration details
- Analysis ID
- 15e52024162e09a6711fbef466190f36
- License Form
- Ministry of Health Medical Device Import No. 015686
- Customs Code
- DHA09401568602
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)
- C3480 Respiratory Fusion Cell Virus Serological Reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 17, 2015
- Expiry Date
- Sep 17, 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" Respiratory Syncytial Virus (RSV) 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 15e52024162e09a6711fbef466190f36 and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices