Pure Global

MONODESIGN lens corrective spectacle lens (Non-sterile)  - Taiwan Registration 539958b80fcbebb67b81ce0accdba9b2

Access comprehensive regulatory information for MONODESIGN lens 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 539958b80fcbebb67b81ce0accdba9b2 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. 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
539958b80fcbebb67b81ce0accdba9b2
Registration Details
Taiwan FDA Registration: 539958b80fcbebb67b81ce0accdba9b2
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

MONODESIGN lens corrective spectacle lens (Non-sterile) 
TW: “聯全”矯正鏡片 (未滅菌)
Risk Class 1
MD

Registration Details

539958b80fcbebb67b81ce0accdba9b2

Ministry of Health Medical Device Import No. 013856

DHA09401385601

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

Feb 18, 2014

Feb 18, 2024