"Quick Test" Respiratory Fusion Cell Virus Rapid Test Reagent (Unsterilized)
Taiwan·Risk Class 1·CERTEST BIOTEC, S.L.·Registered Dec 14, 2016 – Dec 14, 2021Cancelled- Analysis ID
- a14c20bd7f40c69cc62502d1c4e5ce02
- Customs Code
- DHA09401728007
- Manufacturer
- CERTEST BIOTEC, S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- JOLEX INTERNATIONAL CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Respiratory Fusion Cell Virus Serological Reagent (C.3480)".
- 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
- Import Information
- import
- Registration Date
- Dec 14, 2016
- Expiry Date
- Dec 14, 2021
- Cancellation Date
- Mar 15, 2022
- Status
- Logged out
- Reason
- 自請註銷;;屆期未申請展延
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Access comprehensive regulatory information for "Quick Test" Respiratory Fusion Cell Virus 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 a14c20bd7f40c69cc62502d1c4e5ce02 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.