"Dias" Chlamydia pneumoniae IgM antibody kit (unsterilized) - Taiwan Registration f16289eb1ed1c3aab1ff1e49f5afa124
Access comprehensive regulatory information for "Dias" Chlamydia pneumoniae IgM antibody kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f16289eb1ed1c3aab1ff1e49f5afa124 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A. The authorized representative in Taiwan is GRAND MARQUIS 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 limited to the first-level identification scope of Chlamydia serum reagent (C.3120) in the classification and grading management measures for medical devices.
C Immunology and microbiology
C.3120 ๆซ่กฃ่่กๆธ ่ฉฆๅ
import
Dates and Status
May 03, 2013
May 03, 2028