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Pentax Corrective lenses (unsterilized) - Taiwan Registration 8ed1fe7d3526263259c0e89006190406

Access comprehensive regulatory information for Pentax Corrective lenses (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ed1fe7d3526263259c0e89006190406 and manufactured by SEIKO OPTICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is MEITATSU OPTICAL (TAIWAN) 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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8ed1fe7d3526263259c0e89006190406
Registration Details
Taiwan FDA Registration: 8ed1fe7d3526263259c0e89006190406
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Device Details

Pentax Corrective lenses (unsterilized)
TW: ่ณ“ๅพ—ๅฃซ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8ed1fe7d3526263259c0e89006190406

DHA04400929301

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".

M Ophthalmology

M.5844 corrective lenses

import

Dates and Status

Oct 04, 2010

Oct 04, 2015

Apr 25, 2018

Cancellation Information

Logged out

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