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ORIENT Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 8bb9b374389cee83d61dd6262dd5841d

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 8bb9b374389cee83d61dd6262dd5841d and manufactured by FUJITA OPTICAL 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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8bb9b374389cee83d61dd6262dd5841d
Registration Details
Taiwan FDA Registration: 8bb9b374389cee83d61dd6262dd5841d
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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

8bb9b374389cee83d61dd6262dd5841d

Ministry of Health Medical Device Import No. 017022

DHA09401702201

Company Information

Japan

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Sep 22, 2016

Sep 22, 2026

Oct 20, 2022

Cancellation Information

Logged out

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