"Quick Test" Rotavirus-Adenovirus Rapid Test Reagent (Unsterilized)
Taiwan·Risk Class 1·CERTEST BIOTEC S.L.·Registered Feb 13, 2012 – Feb 13, 2017Cancelled- Analysis ID
- 9a99cc01e8d4c4ed476edf7b2f16ff97
- Customs Code
- DHA04401136607
- Manufacturer
- CERTEST BIOTEC S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- JOLEX INTERNATIONAL CO., LTD.
- Intended Use
- It is limited to the first level of identification of "adenovirus serum reagent (C.3020)" and "poliovirus serum reagent (C.3405)" of the medical device management measures.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3020 腺病毒血清試劑;; C.3405 小兒麻痺病毒血清試劑
- Import Information
- import
- Registration Date
- Feb 13, 2012
- Expiry Date
- Feb 13, 2017
- Cancellation Date
- Mar 14, 2017
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Quick Test" Rotavirus-Adenovirus Rapid Test 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 9a99cc01e8d4c4ed476edf7b2f16ff97 and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CERTEST BIOTEC, S.L., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.