Taiwan FDA registration f393e5b59ceb42c703ebdda02db5e835
CICONIA “HCG”
TW: 日本基因喜可妮驗孕試紙
Taiwan·Risk Class 2·MD·NIPPON GENE CO., LTD. Pharmaceutical Toyama Factory·Registered May 25, 2018 – May 25, 2023ExpiredRegistration details
- Analysis ID
- f393e5b59ceb42c703ebdda02db5e835
- License Form
- Ministry of Health Medical Device Import No. 031118
- Customs Code
- DHA05603111802
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUI SHENG INTERNATIONAL CORP.
Product details
- Intended Use
- This product is a simple device that uses a gold-gene immunoassay of monocellular antibodies to detect hCG in urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1155 Human chorionic gonadotropin test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 25, 2018
- Expiry Date
- May 25, 2023
About this record
Access comprehensive regulatory information for CICONIA “HCG” in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f393e5b59ceb42c703ebdda02db5e835 and manufactured by NIPPON GENE CO., LTD. Pharmaceutical Toyama Factory. The authorized representative in Taiwan is HUI SHENG INTERNATIONAL CORP..
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