"Oticon" Kerutron corneal mapper (unsterilized) - Taiwan Registration ed6fac462997968d4aa3b6b2d8585bef
Access comprehensive regulatory information for "Oticon" Kerutron corneal mapper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ed6fac462997968d4aa3b6b2d8585bef and manufactured by OPTIKON 2000 S. P. A. The authorized representative in Taiwan is OPTACT INTERNATIONAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Device Details
Product Details
Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
M Ophthalmology
M.1350 Coratoscope
import
Dates and Status
Mar 21, 2011
Mar 21, 2026
Sep 30, 2021
Cancellation Information
Logged out
่ฝ็บ็ป้ๅญ่