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"Nidek" computerized automatic refractometer (unsterilized) - Taiwan Registration fd5732b2d2b98c97043d9432b70cd156

Access comprehensive regulatory information for "Nidek" computerized automatic refractometer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd5732b2d2b98c97043d9432b70cd156 and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NIDEK CO., LTD., HAMACHO PLANT, 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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fd5732b2d2b98c97043d9432b70cd156
Registration Details
Taiwan FDA Registration: fd5732b2d2b98c97043d9432b70cd156
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Device Details

"Nidek" computerized automatic refractometer (unsterilized)
TW: โ€œๅฐผๅพทๅ…‹โ€้›ป่…ฆ่‡ชๅ‹•ๅผๆŠ˜ๅฐ„่จˆ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

fd5732b2d2b98c97043d9432b70cd156

DHA08402002403

Company Information

Product Details

Limited to the first level identification scope of the "Automatic Ophthalmic Refractive Machine (M.1760)" of the Measures for the Classification and Grading of Medical Equipment.

M Ophthalmology

M.1760 Automatic Ophthalmic Optical Machine

Input;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2025

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