Taiwan FDA registration a3ef4a5621fd74419cea5c40c6f6baee

"EyeSys" Corneal Topography System (Non-Sterile)

TW: "愛視" 角膜地圖儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·EYESYS VISION, INC.·Registered Mar 22, 2016 – Mar 22, 2026Cancelled
Registration details
Analysis ID
a3ef4a5621fd74419cea5c40c6f6baee
License Form
Ministry of Health Medical Device Import No. 016285
Customs Code
DHA09401628502
Company information
Manufacturer Country
United States
Authorized Representative
EVERVISION INSTRUMENT CO.
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1350 Keatoscope
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 22, 2016
Expiry Date
Mar 22, 2026
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "EyeSys" Corneal Topography System (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 a3ef4a5621fd74419cea5c40c6f6baee and manufactured by EYESYS VISION, INC.. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EYESYS VISION, INC., 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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