Taiwan FDA registration 2b389c892d8863c81715e1db7ad17fdb

KODAK corrective spectacle lens (Non-sterile)

TW: KODAK 矯正鏡片 (未滅菌)

Taiwan·Risk Class 1·MD·SIGNET ARMORLITE AMERA PTE. LTD.·Registered Nov 17, 2021 – Nov 17, 2026Active

Registration details

Analysis ID: 2b389c892d8863c81715e1db7ad17fdb
License Form: Ministry of Health Medical Device Import No. 022702
Customs Code: DHA09402270201

Company information

Manufacturer: SIGNET ARMORLITE AMERA PTE. LTD.
Manufacturer Country: Singapore
Authorized Representative: SHIH HENG OPTICAL PTE. LTD. TAIWAN BRANCH (SINGAPORE)

Product details

Intended Use: Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M5844 corrective lenses
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 17, 2021
Expiry Date: Nov 17, 2026

About this record

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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