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ORIENT Corrective spectacle lens (Non-Sterile) - Taiwan Registration 16e6cf8afe4d33394b07cee7baa9c8c3

Access comprehensive regulatory information for ORIENT 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 16e6cf8afe4d33394b07cee7baa9c8c3 and manufactured by CHEMIGLAS CORPORATION. The authorized representative in Taiwan is Roden Optical Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including OPTODEV, INC., FUJITA OPTICAL 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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16e6cf8afe4d33394b07cee7baa9c8c3
Registration Details
Taiwan FDA Registration: 16e6cf8afe4d33394b07cee7baa9c8c3
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Device Details

ORIENT Corrective spectacle lens (Non-Sterile)
TW: ๆฑๆ–น ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

16e6cf8afe4d33394b07cee7baa9c8c3

Ministry of Health Medical Device Import No. 015897

DHA09401589702

Company Information

Korea, Republic of

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Nov 25, 2015

Nov 25, 2020

Jun 22, 2022

Cancellation Information

Logged out

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