"Quick Test" Respiratory Fusion Cell Virus-Adenovirus Rapid Test Reagent (Unsterilized) - Taiwan Registration e018200370acecb0d50238d954a0d56d
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.
Device Details
Product Details
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.
C Immunology and microbiology
C.3480 ๅผๅธ้่ๅ็ดฐ่็ ๆฏ่กๆธ ่ฉฆๅ;; C.3020 ่ บ็ ๆฏ่กๆธ ่ฉฆๅ
import
Dates and Status
Feb 09, 2017
Feb 09, 2022
Mar 09, 2022
Cancellation Information
Logged out
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