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LEADER Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 6b55c069fcbc0ca52dfb6f3da3c6ca78

Access comprehensive regulatory information for LEADER 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 6b55c069fcbc0ca52dfb6f3da3c6ca78 and manufactured by HANMI SWISS OPTICAL CO., LTD.. The authorized representative in Taiwan is Roden Optical Co., Ltd.

This page provides complete technical specifications, regulatory compliance details. 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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6b55c069fcbc0ca52dfb6f3da3c6ca78
Registration Details
Taiwan FDA Registration: 6b55c069fcbc0ca52dfb6f3da3c6ca78
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Device Details

LEADER Corrective Spectacle Lens (Non-Sterile)
TW: ๅ„ท็š„ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

6b55c069fcbc0ca52dfb6f3da3c6ca78

Ministry of Health Medical Device Import No. 017516

DHA09401751600

Company Information

Korea, Republic of

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Feb 22, 2017

Feb 22, 2022

Oct 20, 2022

Cancellation Information

Logged out

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