Pure Global

“SEIKO” Corrective spectacle lens (Non-Sterile) - Taiwan Registration f246ec08c20f11a04f00cf9b627cff33

Access comprehensive regulatory information for “SEIKO” 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 f246ec08c20f11a04f00cf9b627cff33 and manufactured by EHS LENS PHILIPPINES, INC.. The authorized representative in Taiwan is MEGANEICHIBA TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA VISION CARE COMPANY, 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
1 Competitors
1 Recent Registrations
f246ec08c20f11a04f00cf9b627cff33
Registration Details
Taiwan FDA Registration: f246ec08c20f11a04f00cf9b627cff33
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“SEIKO” Corrective spectacle lens (Non-Sterile)
TW: “台灣頂點” 矯正鏡片 (未滅菌)
Risk Class 1
MD

Registration Details

f246ec08c20f11a04f00cf9b627cff33

Ministry of Health Medical Device Import No. 020952

DHA09402095201

Company Information

Philippines

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

Oct 16, 2019

Oct 16, 2024

Companies Making Similar Products
Top companies providing products similar to "“SEIKO” Corrective spectacle lens (Non-Sterile)"