"Quick Test" Respiratory Fusion Cell Virus-Adenovirus Rapid Test Reagent (Unsterilized) - Taiwan Registration 4be235adf51e1a7da5d5d9d5cf4917a4
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 4be235adf51e1a7da5d5d9d5cf4917a4 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.
Device Details
Product Details
It is limited to the first-level identification scope of the medical device management measures "adenovirus serum reagent (C.3020)" and "respiratory fusion cell virus serum reagent (C.3480)".
C Immunology and microbiology
C.3480 ๅผๅธ้่ๅ็ดฐ่็ ๆฏ่กๆธ ่ฉฆๅ;; C.3020 ่ บ็ ๆฏ่กๆธ ่ฉฆๅ
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Dates and Status
Feb 21, 2012
Feb 21, 2017
Mar 09, 2017
Cancellation Information
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