Fukushima Chlamydomydia rapid immunochromatography assay - Taiwan Registration 575c3c7555ed344de9f8d8fc14992f15
Access comprehensive regulatory information for Fukushima Chlamydomydia rapid immunochromatography assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 575c3c7555ed344de9f8d8fc14992f15 and manufactured by VEDA LAB. The authorized representative in Taiwan is Fukushima Medical Equipment 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
It is used to detect Chlamydia infection in the endocervical lining of the uterus.
C Immunology and microbiology
C.3120 ๆซ่กฃ่่กๆธ ่ฉฆๅ
import
Dates and Status
Dec 22, 2005
Dec 22, 2010
Nov 20, 2012
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ