Taiwan FDA registration 783c2448cbf07078c5d25f2a2367f688

"Nidek" optical path phase contrast meter (unsterilized)

TW: "尼德克" 光路徑相差儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·NIDEK CO., LTD. HAMACHO PLANT·Registered Apr 29, 2011 – Apr 29, 2026Cancelled
Registration details
Analysis ID
783c2448cbf07078c5d25f2a2367f688
Customs Code
DHA04401029008
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
QMS/QSD;; 輸入
Dates and status
Registration Date
Apr 29, 2011
Expiry Date
Apr 29, 2026
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" optical path phase contrast meter (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 783c2448cbf07078c5d25f2a2367f688 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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