Rapid Test Reagent for Influenza Virus A and B (Unsterilized) - Taiwan Registration 3f49279c01150054b056e1c1d0e5409e
Access comprehensive regulatory information for Rapid Test Reagent for Influenza Virus A and B (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f49279c01150054b056e1c1d0e5409e and manufactured by Kaiwu Technology Co., Ltd. Nanke Factory. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Nanke Factory.
This page provides complete technical specifications, regulatory compliance details. 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 influenza virus serum reagent (C.3330) in the classification and grading management measures for medical devices.
C Immunology and microbiology
C.3330 ๆตๆ็ ๆฏ่กๆธ ่ฉฆๅ
Domestic
Dates and Status
Jan 27, 2014
Jan 27, 2024

