Taiwan FDA registration 64f7c6d1c5d02e977a2acbdf540e0f1d
"GHope" Legionella (Non-Sterile)
TW: "炬合" 退伍軍人肺炎尿液抗原快速診斷試劑 (未滅菌)
Taiwan·Risk Class 1·MD·EIKEN CHEMICAL CO., LTD.·Registered Jul 25, 2018 – Jul 25, 2023CancelledRegistration details
- Analysis ID
- 64f7c6d1c5d02e977a2acbdf540e0f1d
- License Form
- Ministry of Health Medical Device Import No. 019413
- Customs Code
- DHA09401941300
Company information
- Manufacturer
- EIKEN CHEMICAL CO., LTD.
- 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)
- C3300 Haemophilus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 25, 2018
- Expiry Date
- Jul 25, 2023
- Cancellation Date
- Jan 28, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "GHope" Legionella (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 64f7c6d1c5d02e977a2acbdf540e0f1d and manufactured by EIKEN CHEMICAL CO., LTD.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..
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