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NIDEK corrective spectacle lens(Non-sterile) - Taiwan Registration bba4d5e4cd483ecc4baf8d36450fda4f

Access comprehensive regulatory information for NIDEK 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 bba4d5e4cd483ecc4baf8d36450fda4f and manufactured by CHEMILENS CO., LTD.. The authorized representative in Taiwan is SHIH HENG OPTICAL PTE. LTD. TAIWAN BRANCH (SINGAPORE).

This page provides complete technical specifications, regulatory compliance details. 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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Registration Details
Taiwan FDA Registration: bba4d5e4cd483ecc4baf8d36450fda4f
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Device Details

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

Registration Details

bba4d5e4cd483ecc4baf8d36450fda4f

Ministry of Health Medical Device Import No. 013501

DHA09401350103

Company Information

Korea, Republic of

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Oct 16, 2013

Oct 16, 2018

Jun 07, 2022

Cancellation Information

Logged out

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