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TOYOLENS Corrective spectacle lens (Non-sterile)  - Taiwan Registration ae71c55d3669188f516b4ec53efc85bd

Access comprehensive regulatory information for TOYOLENS 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 ae71c55d3669188f516b4ec53efc85bd and manufactured by FUJITA OPTICAL CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RODENSTOCK GMBH, and 1 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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ae71c55d3669188f516b4ec53efc85bd
Registration Details
Taiwan FDA Registration: ae71c55d3669188f516b4ec53efc85bd
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Device Details

TOYOLENS Corrective spectacle lens (Non-sterile) 
TW: 東洋 矯正鏡片 (未滅菌)
Risk Class 1
MD

Registration Details

ae71c55d3669188f516b4ec53efc85bd

Ministry of Health Medical Device Import No. 013588

DHA09401358802

Company Information

Japan

Product Details

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

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Nov 14, 2013

Nov 14, 2023

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