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"Nidek" manual refractometer (unsterilized) - Taiwan Registration bc5141b671abb592973c460bd6dd484e

Access comprehensive regulatory information for "Nidek" manual 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 bc5141b671abb592973c460bd6dd484e 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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bc5141b671abb592973c460bd6dd484e
Registration Details
Taiwan FDA Registration: bc5141b671abb592973c460bd6dd484e
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Device Details

"Nidek" manual refractometer (unsterilized)
TW: โ€œๅฐผๅพทๅ…‹โ€ๆ‰‹ๅ‹•ๆŠ˜ๅฐ„่จˆ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

bc5141b671abb592973c460bd6dd484e

DHA08400819302

Company Information

Product Details

It is limited to the first-level identification scope of the "Manual Refractor (M.1770)" of the Administrative Measures for the Classification and Grading of Medical Devices.

M Ophthalmology

M.1770 ๆ‰‹ๅ‹•ๅผ้ฉ—ๅ…‰ๅ„€

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Oct 01, 2021

Oct 31, 2025

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