"Quick Test" Respiratory Fusion Cell Virus-Adenovirus Rapid Test Reagent (Unsterilized)
Taiwan·Risk Class 1·CERTEST BIOTEC, S.L.·Registered Feb 09, 2017 – Feb 09, 2022Cancelled- Analysis ID
- e018200370acecb0d50238d954a0d56d
- Customs Code
- DHA09401748002
- 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 "respiratory fusion cell virus serum reagent (C.3480)" under the management measures for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3480 呼吸道融合細胞病毒血清試劑;; C.3020 腺病毒血清試劑
- Import Information
- import
- Registration Date
- Feb 09, 2017
- Expiry Date
- Feb 09, 2022
- Cancellation Date
- Mar 09, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Quick Test" Respiratory Fusion Cell Virus-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 e018200370acecb0d50238d954a0d56d 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.