"Quick Test" Rotavirus-Adenovirus Rapid Test Reagent (Unsterilized)
Taiwan·Risk Class 1·CERTEST BIOTEC, S.L.·Registered Jan 23, 2017 – Jan 23, 2022Cancelled- Analysis ID
- a4969feb0a8a1d550db3a090eecda732
- Customs Code
- DHA09401745108
- Manufacturer
- CERTEST BIOTEC, S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- JOLEX INTERNATIONAL CO., LTD.
- Intended Use
- Limited to the first level of identification range of "adenovirus serum reagent (C.3020)" and "polio virus serum reagent (C.3405)" under the management measures for medical devices.
- 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
- Jan 23, 2017
- Expiry Date
- Jan 23, 2022
- Cancellation Date
- Mar 08, 2022
- Status
- Logged out
- Reason
- 自請註銷
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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 a4969feb0a8a1d550db3a090eecda732 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.