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PENTAX corrective spectacle lens (Non-Sterile) - Taiwan Registration c0cdd462075991bbff871825c4f384b0

Access comprehensive regulatory information for PENTAX 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 c0cdd462075991bbff871825c4f384b0 and manufactured by HOYA LENS MANUFACTURING PHILIPPINES INC.. The authorized representative in Taiwan is HOYA LENS TAIWAN 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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c0cdd462075991bbff871825c4f384b0
Registration Details
Taiwan FDA Registration: c0cdd462075991bbff871825c4f384b0
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Device Details

PENTAX corrective spectacle lens (Non-Sterile)
TW: ่ณ“ๅพทๅ…‹ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

c0cdd462075991bbff871825c4f384b0

Ministry of Health Medical Device Import No. 014255

DHA09401425506

Company Information

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Jun 16, 2014

Jun 16, 2019

Jun 22, 2022

Cancellation Information

Logged out

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