Pure Global

FUJI LENS Corrective Spectacle Lens (Non-sterile)  - Taiwan Registration 6de913437c589b5e516a6ca68341421c

Access comprehensive regulatory information for FUJI 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 6de913437c589b5e516a6ca68341421c and manufactured by ASAHI LITE 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
6de913437c589b5e516a6ca68341421c
Registration Details
Taiwan FDA Registration: 6de913437c589b5e516a6ca68341421c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

FUJI LENS Corrective Spectacle Lens (Non-sterile) 
TW: 富吉仕 矯正鏡片 (未滅菌)
Risk Class 1
MD

Registration Details

6de913437c589b5e516a6ca68341421c

Ministry of Health Medical Device Import No. 013583

DHA09401358305

Company Information

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

Nov 13, 2013

Nov 13, 2023