Wonderford Influenza A/B Virus Rapid Test Reagent (Unsterilized) - Taiwan Registration b198b5a0155a0c480b3d139d7621aa91
Access comprehensive regulatory information for Wonderford Influenza A/B 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 b198b5a0155a0c480b3d139d7621aa91 and manufactured by WONDFO BIOTECH CO., LTD. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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
Chinese goods;; input
Dates and Status
Sep 30, 2009
Sep 30, 2024

