Taiwan FDA registration fd5732b2d2b98c97043d9432b70cd156

"Nidek" computerized automatic refractometer (unsterilized)

TW: “尼德克”電腦自動式折射計(未滅菌)
Taiwan flagTaiwan·Risk Class 1·NIDEK CO., LTD., HAMACHO PLANT·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
fd5732b2d2b98c97043d9432b70cd156
Customs Code
DHA08402002403
Company information
Manufacturer Country
Japan
Authorized Representative
IKI MEDICAL CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the "Automatic Ophthalmic Refractive Machine (M.1760)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.1760 Automatic Ophthalmic Optical Machine
Import Information
Input;; QMS/QSD
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 "Nidek" computerized automatic 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 fd5732b2d2b98c97043d9432b70cd156 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.

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