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PENTAX Optical corrective spectacle lens (Non-Sterile) - Taiwan Registration 8dc1e15626d37a56e6c95de8d31393fe

Access comprehensive regulatory information for PENTAX Optical 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 8dc1e15626d37a56e6c95de8d31393fe and manufactured by HOYA LENS MANUFACTURING PHILIPPINES INC.. The authorized representative in Taiwan is Wansheng Trading Co., Ltd.

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8dc1e15626d37a56e6c95de8d31393fe
Registration Details
Taiwan FDA Registration: 8dc1e15626d37a56e6c95de8d31393fe
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Device Details

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

Registration Details

8dc1e15626d37a56e6c95de8d31393fe

Ministry of Health Medical Device Import No. 017144

DHA09401714402

Company Information

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Nov 02, 2016

Nov 02, 2021

Sep 05, 2019

Cancellation Information

Logged out

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