“Diasorin” Chlamydia MIF IgM Kit (Non sterile) - Taiwan Registration 582f720e506172f155434d655b49bda4
Access comprehensive regulatory information for “Diasorin” Chlamydia MIF IgM Kit (Non sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 582f720e506172f155434d655b49bda4 and manufactured by DiaSorin Molecular LLC. The authorized representative in Taiwan is FENG CHI BIOTECH 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
Registration Details
582f720e506172f155434d655b49bda4
Ministry of Health Medical Device Import No. 020369
DHA09402036907
Product Details
Limited to the first level identification range of Chlamydomydia serum reagent (C.3120) of medical device management methods.
C Immunology and microbiology devices
C3120 Chlamydia serum reagent
Imported from abroad
Dates and Status
Apr 25, 2019
Apr 25, 2024

