Taiwan FDA registration 53cb9c36a530a0a4efd188bf2ac7c23f

"New Japan" ophthalmic refractive machine (unsterilized)

TW: “新日本” 眼科用驗光機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·REXXAM CO., LTD. KAGAWA FACTORY·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
53cb9c36a530a0a4efd188bf2ac7c23f
Customs Code
DHA08402178201
Company information
Manufacturer Country
Japan
Authorized Representative
TAIWAN INSTRUMENT 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
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 "New Japan" ophthalmic refractive machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 53cb9c36a530a0a4efd188bf2ac7c23f and manufactured by REXXAM CO., LTD. KAGAWA FACTORY. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including REXXAM CO., LTD. KAGAWA FACTORY, 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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