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LEESAM corrective spectacle lens (Non-Sterile) - Taiwan Registration e5a6c06a1aae62f6a31224520676dbf1

Access comprehensive regulatory information for LEESAM 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 e5a6c06a1aae62f6a31224520676dbf1 and manufactured by ITOLENS CO., LTD.. The authorized representative in Taiwan is LEESAM OPT-TECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NIPPON LENS INDUSTRIAL CO., LTD., 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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e5a6c06a1aae62f6a31224520676dbf1
Registration Details
Taiwan FDA Registration: e5a6c06a1aae62f6a31224520676dbf1
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Device Details

LEESAM corrective spectacle lens (Non-Sterile)
TW: ็ซ‹ๅ‹ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e5a6c06a1aae62f6a31224520676dbf1

Ministry of Health Medical Device Import No. 020503

DHA09402050301

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

May 30, 2019

May 30, 2024

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