"Nidek" manual refractometer (unsterilized) - Taiwan Registration 967bb8826237e8ba858fbdfefe41bbc2
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 967bb8826237e8ba858fbdfefe41bbc2 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.
Device Details
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Manual Refractometer (M.1770)".
M Ophthalmology
M.1770 ๆๅๅผ้ฉๅ ๅ
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Oct 08, 2009
Oct 08, 2024
Sep 30, 2021
Cancellation Information
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