"Ikrimicus" Klebsiella pneumoniae K1/K2 serotyping quick screening card (unsterilized) - Taiwan Registration 0343684958652fb048c54eec29a5fbab
Access comprehensive regulatory information for "Ikrimicus" Klebsiella pneumoniae K1/K2 serotyping quick screening card (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0343684958652fb048c54eec29a5fbab and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is KEMYTH BIOTECH CO., LTD..
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
Limited to the first level identification range of the Administrative Measures for Medical Devices "Klebsiella serological reagent (C.3340)".
C Immunology and microbiology
C.3340 ๅ ้ท็ฝๆฐๆกฟ่ๅฑฌ่กๆธ ่ฉฆๅ
Domestic;; Contract manufacturing
Dates and Status
Nov 13, 2017
Nov 13, 2022
Apr 12, 2024
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ