Pure Global

“GANESHA & DEVICE”corrective spectacle lens(Non-sterile) - Taiwan Registration d16662d360b0b6ec99f41dbd3ef48475

Access comprehensive regulatory information for “GANESHA & DEVICE”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 d16662d360b0b6ec99f41dbd3ef48475 and manufactured by DAEMYUNG OPTICAL CO. LTD.. The authorized representative in Taiwan is YI JIA YI OPTICAL 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
d16662d360b0b6ec99f41dbd3ef48475
Registration Details
Taiwan FDA Registration: d16662d360b0b6ec99f41dbd3ef48475
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“GANESHA & DEVICE”corrective spectacle lens(Non-sterile)
TW: “迦納夏”矯正鏡片 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

d16662d360b0b6ec99f41dbd3ef48475

Ministry of Health Medical Device Import No. 013618

DHA09401361801

Company Information

Korea, Republic of

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Nov 21, 2013

Nov 21, 2018

Aug 30, 2022

Cancellation Information

Logged out

未展延而逾期者