Taiwan FDA registration 68175eb361b6b25704b8f779b15cf668
"SEIKEN"QuickNavi-Norovirus 2
TW: “生研”諾羅病毒快速檢驗套組
Taiwan·Risk Class 2·MD·DENKA CO., LTD·Registered Aug 07, 2015 – Aug 07, 2025ExpiredRegistration details
- Analysis ID
- 68175eb361b6b25704b8f779b15cf668
- License Form
- Ministry of Health Medical Device Import No. 027544
- Customs Code
- DHA05602754401
Company information
- Manufacturer
- DENKA CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- This product is used to detect norovirus antigen in human stool samples.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3395 Norovirus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 07, 2015
- Expiry Date
- Aug 07, 2025
About this record
Access comprehensive regulatory information for "SEIKEN"QuickNavi-Norovirus 2 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68175eb361b6b25704b8f779b15cf668 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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