"Nidek" manual refractometer (unsterilized)
Taiwan·Risk Class 1·NIDEK CO., LTD. HAMACHO PLANT·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- bc5141b671abb592973c460bd6dd484e
- Customs Code
- DHA08400819302
- Manufacturer
- NIDEK CO., LTD. HAMACHO PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
- Intended Use
- 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.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1770 手動式驗光儀
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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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.