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ORIENT Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 8d0baa6eb106677566fca70bd47ca4f8

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 8d0baa6eb106677566fca70bd47ca4f8 and manufactured by ESSILOR MANUFACTURING (THAILAND) CO., LTD.. 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., 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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8d0baa6eb106677566fca70bd47ca4f8
Registration Details
Taiwan FDA Registration: 8d0baa6eb106677566fca70bd47ca4f8
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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

8d0baa6eb106677566fca70bd47ca4f8

Ministry of Health Medical Device Import No. 016633

DHA09401663309

Company Information

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Jun 07, 2016

Jun 07, 2021

Oct 20, 2022

Cancellation Information

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