Taiwan FDA registration ae71c55d3669188f516b4ec53efc85bd

TOYOLENS Corrective spectacle lens (Non-sterile) 

TW: 東洋 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·FUJITA OPTICAL CO., LTD.·Registered Nov 14, 2013 – Nov 14, 2023Expired
Registration details
Analysis ID
ae71c55d3669188f516b4ec53efc85bd
License Form
Ministry of Health Medical Device Import No. 013588
Customs Code
DHA09401358802
Company information
Manufacturer Country
Japan
Authorized Representative
HKO OPTICAL LENS (TAIWAN) CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M5844 corrective lenses
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 14, 2013
Expiry Date
Nov 14, 2023
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About this record

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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