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"Righton" Auto Optester (non-sterile) - Taiwan Registration 2e0f1cc165158ffde6b705693fbdc270

Access comprehensive regulatory information for "Righton" Auto Optester (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 2e0f1cc165158ffde6b705693fbdc270 and manufactured by TOHOKU RIGHT MFG. CO., LTD. OHSATO FACTORY. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..

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2e0f1cc165158ffde6b705693fbdc270
Registration Details
Taiwan FDA Registration: 2e0f1cc165158ffde6b705693fbdc270
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Device Details

"Righton" Auto Optester (non-sterile)
TW: "่Š็™ป"้›ปๅ‹•่‡ช่ฆบๅผ้ฉ—ๅ…‰ๅ„€(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2e0f1cc165158ffde6b705693fbdc270

Ministry of Health Medical Device Import Registration No. 003133

DHA08400313301

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices (Manual Refractometer (M.1770).

M Ophthalmic devices

M1770 Manual refractometer

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026