Taiwan FDA registration 2e0f1cc165158ffde6b705693fbdc270

"Righton" Auto Optester (non-sterile)

TW: "萊登"電動自覺式驗光儀(未滅菌)

Taiwan·Risk Class 1·MD·TOHOKU RIGHT MFG. CO., LTD. OHSATO FACTORY·Registered Oct 01, 2021 – Oct 31, 2026Active

Registration details

Analysis ID: 2e0f1cc165158ffde6b705693fbdc270
License Form: Ministry of Health Medical Device Import Registration No. 003133
Customs Code: DHA08400313301

Company information

Manufacturer: TOHOKU RIGHT MFG. CO., LTD. OHSATO FACTORY
Manufacturer Country: Japan
Authorized Representative: TAIWAN OPTICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices (Manual Refractometer (M.1770).
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M1770 Manual refractometer
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2026

About this record

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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