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"GULDEN" Ophthalmic bar prism (Non-Sterile) - Taiwan Registration c580122d4ddf81e18c61405e267ba57b

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 c580122d4ddf81e18c61405e267ba57b and manufactured by GULDEN OPHTHALMICS. The authorized representative in Taiwan is HATCHELL CO., LTD..

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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c580122d4ddf81e18c61405e267ba57b
Registration Details
Taiwan FDA Registration: c580122d4ddf81e18c61405e267ba57b
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Device Details

"GULDEN" Ophthalmic bar prism (Non-Sterile)
TW: "ๅค็™ป" ็œผ็ง‘็”จๆฃ’็‹€็จœ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c580122d4ddf81e18c61405e267ba57b

Ministry of Health Medical Device Import No. 022112

DHA09402211206

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

Nov 16, 2020

Nov 16, 2025

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