Taiwan FDA registration bfbef88b562a921f1c6475a2e17d1af3
Willotic rotavirus (ROTA) reagent (unsterilized)
TW: 威洛鐵克輪狀病毒(ROTA)試劑(未滅菌)
Taiwan·Risk Class 1·OMEGA DIAGNOSTICS LTD.·Registered Nov 17, 2005 – Nov 17, 2020CancelledRegistration details
- Analysis ID
- bfbef88b562a921f1c6475a2e17d1af3
- Customs Code
- DHA04400199302
Company information
- Manufacturer
- OMEGA DIAGNOSTICS LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- Detection of rotavirus in stool.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3405 Poliomyelitis virus serum reagent
- Import Information
- import
Dates and status
- Registration Date
- Nov 17, 2005
- Expiry Date
- Nov 17, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Willotic rotavirus (ROTA) reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bfbef88b562a921f1c6475a2e17d1af3 and manufactured by OMEGA DIAGNOSTICS LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
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