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"Schiff" Corrective spectacle lens (Non-Sterile) - Taiwan Registration 954787fa82e984034ef3bec6644c7d49

Access comprehensive regulatory information for "Schiff" 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 954787fa82e984034ef3bec6644c7d49 and manufactured by WENZHOU EYEWORKS IMP. & EXP. CO, LTD. The authorized representative in Taiwan is SCHIFF INTERNATIONAL CO..

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954787fa82e984034ef3bec6644c7d49
Registration Details
Taiwan FDA Registration: 954787fa82e984034ef3bec6644c7d49
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Device Details

"Schiff" Corrective spectacle lens (Non-Sterile)
TW: "ไธ€ๅ”็ด€" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

954787fa82e984034ef3bec6644c7d49

Ministry of Health Medical Device Land Transport No. 004679

DHA09600467907

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; Made in China

Dates and Status

Oct 06, 2022

Oct 06, 2027