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"Iridex" Gonioscopic Prism (non-sterile) - Taiwan Registration 68690b1388bed0b94232607e238a99c9

Access comprehensive regulatory information for "Iridex" Gonioscopic 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 68690b1388bed0b94232607e238a99c9 and manufactured by OCULAR INSTRUMENTS, INC.. The authorized representative in Taiwan is CLINICO INC..

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.

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68690b1388bed0b94232607e238a99c9
Registration Details
Taiwan FDA Registration: 68690b1388bed0b94232607e238a99c9
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Device Details

"Iridex" Gonioscopic Prism (non-sterile)
TW: "่‰พ็‘žๆ–ฏ" ่ฆ–่ปธ่ง’ๅบฆ็จœ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

68690b1388bed0b94232607e238a99c9

Ministry of Health Medical Device Import No. 016745

DHA09401674507

Company Information

United States

Product Details

Limited to the first level recognition range of the visual axis angle prism (M.1660) of the medical equipment management measures.

M Ophthalmic devices

M1660 axis angle prism

Imported from abroad

Dates and Status

Jul 06, 2016

Jul 06, 2026