Taiwan FDA registration 5607a9cff879ae47770cfefc30405a5d

"Rexxam" Corneal Topographer (Non-Sterile)

TW: "隆祥" 角膜地圖儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·REXXAM CO., LTD. KAGAWA FACTORY·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
5607a9cff879ae47770cfefc30405a5d
License Form
Ministry of Health Medical Device Import Registration No. 021478
Customs Code
DHA08402147808
Company information
Manufacturer Country
Japan
Authorized Representative
TAIWAN INSTRUMENT CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1350 Keatoscope
Import Information
Imported from abroad
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 "Rexxam" Corneal Topographer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5607a9cff879ae47770cfefc30405a5d 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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