Taiwan FDA registration 3d0cf40093379317fb3a7dcd6bb19335

"VISIA" Corneal Topographer (Non-Sterile)

TW: "美視雅" 角膜地圖儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·VISIA IMAGING S.R.L.·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
3d0cf40093379317fb3a7dcd6bb19335
License Form
Ministry of Health Medical Device Import Registration No. 015954
Customs Code
DHA08401595402
Company information
Manufacturer Country
Italy
Authorized Representative
YU TA TRADING 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, 2026
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About this record

Access comprehensive regulatory information for "VISIA" 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 3d0cf40093379317fb3a7dcd6bb19335 and manufactured by VISIA IMAGING S.R.L.. The authorized representative in Taiwan is YU TA TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VISIA IMAGING S.R.L., 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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