Taiwan FDA registration 22b1f8747a7b554ab8f5df766f581144

"Flyshuttle" corrective lenses (unsterilized)

TW: "飛梭" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SEE WORLD OPTICAL CO., LTD·Registered Jul 21, 2017 – Jul 21, 2027Active
Registration details
Analysis ID
22b1f8747a7b554ab8f5df766f581144
Customs Code
DHA09600315000
Company information
Manufacturer Country
China
Authorized Representative
ESSILOR-POLYLITE TAIWAN CO., LTD.
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)
M.5844 corrective lenses
Import Information
Chinese goods;; input
Dates and status
Registration Date
Jul 21, 2017
Expiry Date
Jul 21, 2027
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About this record

Access comprehensive regulatory information for "Flyshuttle" corrective lenses (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 22b1f8747a7b554ab8f5df766f581144 and manufactured by SEE WORLD OPTICAL CO., LTD. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including CHEMIGLAS CORPORATION, ESSILOR MANUFACTURING (THAILAND) CO., LTD., and 5 recent registrations in the same category. 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.

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