Pure Global

ORIENT Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration c168c6031edb1b2db0b37443da56cafa

Access comprehensive regulatory information for ORIENT 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 c168c6031edb1b2db0b37443da56cafa and manufactured by OPTODEV, INC.. The authorized representative in Taiwan is Roden Optical Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including CHEMIGLAS CORPORATION, OPTODEV, INC., and 5 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
5 Competitors
5 Recent Registrations
c168c6031edb1b2db0b37443da56cafa
Registration Details
Taiwan FDA Registration: c168c6031edb1b2db0b37443da56cafa
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

ORIENT Corrective Spectacle Lens (Non-Sterile)
TW: ๆฑๆ–น็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

c168c6031edb1b2db0b37443da56cafa

Ministry of Health Medical Device Import No. 021595

DHA09402159508

Company Information

Philippines

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

May 29, 2020

May 29, 2025

Oct 20, 2022

Cancellation Information

Logged out

ๅ…ฌๅธๆญ‡ๆฅญ