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"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.

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cef54a5624e67610df72fabcb845a2b8
Registration Details
Taiwan FDA Registration: cef54a5624e67610df72fabcb845a2b8
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Device Details

"Gulden" Ophthalmic Bar Prism (Non-Sterile)
TW: "ๅŸบ็ˆพๅพท"็œผ็ง‘็”จๆฃ’็‹€็จœ้ก(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

cef54a5624e67610df72fabcb845a2b8

Ministry of Health Medical Device Import No. 018375

DHA09401837500

Company Information

United States

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

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