Synctoplasma pneumonia antibody reagent (unsterilized) - Taiwan Registration 05cb10e2b19520bb66805d5969fe2984
Access comprehensive regulatory information for Synctoplasma pneumonia antibody 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 05cb10e2b19520bb66805d5969fe2984 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL 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 classification and grading management method of medical equipment, the first level identification range of "Mycoplasma serum reagent (C.3375)".
C Immunology and microbiology
C.3375 ้ปดๆผฟ่ๅฑฌ่กๆธ ่ฉฆๅ
import
Dates and Status
Oct 19, 2010
Oct 19, 2025

