"Keeler" Magnification Loupes and accessories(Non-Sterile) - Taiwan Registration 2bee5703b0fe7ee3a46ea2e693054e35
Access comprehensive regulatory information for "Keeler" Magnification Loupes and accessories(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 2bee5703b0fe7ee3a46ea2e693054e35 and manufactured by KEELER LTD.. The authorized representative in Taiwan is TAIWAN 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.
Device Details
Registration Details
2bee5703b0fe7ee3a46ea2e693054e35
Ministry of Health Medical Device Import Registration No. 003280
DHA08400328001
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices (Ophthalmic Surgical Glasses [M.4770]).
M Ophthalmic devices
M4770 Ophthalmic surgical glasses (magnifying glasses)
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2026