Taiwan FDA registration e140a36239b49afd5985890a7e73df2c

"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 Jan 15, 2019 – Jan 15, 2024Cancelled
Registration details
Analysis ID
e140a36239b49afd5985890a7e73df2c
Customs Code
DHA09402002402
Company information
Manufacturer Country
Japan
Authorized Representative
IKI MEDICAL CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of ophthalmic optometry machine (M.1760) of the management measures for 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
Jan 15, 2019
Expiry Date
Jan 15, 2024
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 e140a36239b49afd5985890a7e73df2c 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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