"Lunell" manual refractometer (unsterilized)
Taiwan·Risk Class 1·LUNEAU TECHNOLOGY OPERATIONS·Registered Oct 22, 2020 – Oct 22, 2025Cancelled- Analysis ID
- e441364f623589ee3baae9aee2831dc2
- Customs Code
- DHA09402205405
- Manufacturer
- LUNEAU TECHNOLOGY OPERATIONS
- Manufacturer Country
- France
- Authorized Representative
- JUN FENG OPTICAL 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 22, 2020
- Expiry Date
- Oct 22, 2025
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Lunell" 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 e441364f623589ee3baae9aee2831dc2 and manufactured by LUNEAU TECHNOLOGY OPERATIONS. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LUNEAU TECHNOLOGY OPERATIONS, 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.