Taiwan FDA registration 399e78815a706bdfc616efc1195f7635

"Lunell" manual refractometer (unsterilized)

TW: "路尼耳" 手動折射計 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·LUNEAU TECHNOLOGY OPERATIONS·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
399e78815a706bdfc616efc1195f7635
Customs Code
DHA08402205409
Company information
Manufacturer Country
France
Authorized Representative
JUN FENG OPTICAL CO., LTD.
Product details
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
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

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 399e78815a706bdfc616efc1195f7635 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.

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