"Gulden" Ophthalmic Bar Prism (Non-Sterile) - Taiwan Registration cef54a5624e67610df72fabcb845a2b8
Access comprehensive regulatory information for "Gulden" Ophthalmic Bar Prism (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 cef54a5624e67610df72fabcb845a2b8 and manufactured by GULDEN OPHTHALMICS. The authorized representative in Taiwan is FORESIGHT ASSISTIVE TECHNOLOGY INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GULDEN OPHTHALMICS, and 1 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.
Device Details
Registration Details
cef54a5624e67610df72fabcb845a2b8
Ministry of Health Medical Device Import No. 018375
DHA09401837500
Product Details
Limited to the first level recognition range of rod prism (M.1650) for ophthalmology under the management measures for medical equipment.
M Ophthalmic devices
M1650 Rod prism for ophthalmology
Imported from abroad
Dates and Status
Oct 03, 2017
Oct 03, 2027

