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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).

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2b389c892d8863c81715e1db7ad17fdb
Registration Details
Taiwan FDA Registration: 2b389c892d8863c81715e1db7ad17fdb
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Device Details

KODAK corrective spectacle lens (Non-sterile)
TW: KODAK ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2b389c892d8863c81715e1db7ad17fdb

Ministry of Health Medical Device Import No. 022702

DHA09402270201

Company Information

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