"Nidek" manual refractometer (unsterilized)
Taiwan·Risk Class 1·NIDEK CO., LTD. HAMACHO PLANT·Registered Oct 08, 2009 – Oct 08, 2024Cancelled- Analysis ID
- 967bb8826237e8ba858fbdfefe41bbc2
- Customs Code
- DHA04400819305
- Manufacturer
- NIDEK CO., LTD. HAMACHO PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
- 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 Ophthalmology
- Product Type (Level 2)
- M.1770 手動式驗光儀
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Oct 08, 2009
- Expiry Date
- Oct 08, 2024
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 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.