Taiwan FDA registration e2fdb1d3e009ee72ec7e18115f542b4a

"Bindeck" corrective lenses (unsterilized)

TW: "賓德克" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SHANGHAI CONANT OPTICS CO., LTD·Registered Dec 07, 2018 – Dec 07, 2028Active
Registration details
Analysis ID
e2fdb1d3e009ee72ec7e18115f542b4a
Customs Code
DHA09600362709
Company information
Manufacturer Country
China
Authorized Representative
HOYA LENS TAIWAN 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
Input;; Chinese goods
Dates and status
Registration Date
Dec 07, 2018
Expiry Date
Dec 07, 2028
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About this record

Access comprehensive regulatory information for "Bindeck" 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 e2fdb1d3e009ee72ec7e18115f542b4a and manufactured by SHANGHAI CONANT OPTICS CO., LTD. The authorized representative in Taiwan is HOYA LENS TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DAEJEON DAEMYUNG OPTICAL (HANGZHOU) CO.,LTD., and 1 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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