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ORIENT Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration ce6b902c142ee390c4bcd79649f5f4bf

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 ce6b902c142ee390c4bcd79649f5f4bf and manufactured by JP OPTICAL PTE 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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ce6b902c142ee390c4bcd79649f5f4bf
Registration Details
Taiwan FDA Registration: ce6b902c142ee390c4bcd79649f5f4bf
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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

ce6b902c142ee390c4bcd79649f5f4bf

Ministry of Health Medical Device Manufacturing No. 007106

Company Information

Taiwan, Province of China

Product Details

M Ophthalmic devices

M5844 corrective lenses

Produced in Taiwan, China; Contract manufacturing

Dates and Status

Feb 08, 2018

Feb 08, 2023

Oct 20, 2022

Cancellation Information

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