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ORIENT Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration d47085e3f727cdbfc996998c436b403c

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 d47085e3f727cdbfc996998c436b403c and manufactured by OPTODEV, INC.. The authorized representative in Taiwan is Roden Optical Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including OPTODEV, INC., CHEMIGLAS CORPORATION, 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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d47085e3f727cdbfc996998c436b403c
Registration Details
Taiwan FDA Registration: d47085e3f727cdbfc996998c436b403c
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Device Details

ORIENT Corrective Spectacle Lens (Non-Sterile)
TW: ๆฑๆ–น็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

d47085e3f727cdbfc996998c436b403c

Ministry of Health Medical Device Import No. 014834

DHA09401483409

Company Information

Philippines

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Jan 09, 2015

Jan 09, 2020

Jun 22, 2022

Cancellation Information

Logged out

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