KODAK corrective spectacle lens (Non-sterile) - Taiwan Registration 2b389c892d8863c81715e1db7ad17fdb
Access comprehensive regulatory information for KODAK corrective spectacle lens (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 2b389c892d8863c81715e1db7ad17fdb and manufactured by SIGNET ARMORLITE AMERA PTE. LTD.. The authorized representative in Taiwan is SHIH HENG OPTICAL PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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
2b389c892d8863c81715e1db7ad17fdb
Ministry of Health Medical Device Import No. 022702
DHA09402270201
Product Details
Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.
M Ophthalmology
M5844 corrective lenses
Imported from abroad
Dates and Status
Nov 17, 2021
Nov 17, 2026

