Taiwan FDA registration ac8ee4174ddee3c28a6c83f11da21ea4
"GHope" Streptococcus Pneumoniae Kit (Non-Sterile)
TW: "炬合" 肺炎鏈球菌檢驗試劑組 (未滅菌)
Registration details
- Analysis ID
- ac8ee4174ddee3c28a6c83f11da21ea4
- License Form
- Ministry of Health Medical Device Import No. 019414
- Customs Code
- DHA09401941402
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)
- C3740 Streptococcus 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" Streptococcus Pneumoniae 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 ac8ee4174ddee3c28a6c83f11da21ea4 and manufactured by EIKEN CHEMICAL CO., LTD.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..
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