"TAKAGI" Keratometer (Non-Sterile) - Taiwan Registration 9b9c24083f982e0f837c1bf2a4bdedaf
Access comprehensive regulatory information for "TAKAGI" Keratometer (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 9b9c24083f982e0f837c1bf2a4bdedaf and manufactured by TAKAGI SEIKO CO., LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TAKAGI SEIKO CO., LTD., 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.
Device Details
Registration Details
9b9c24083f982e0f837c1bf2a4bdedaf
Ministry of Health Medical Device Import Registration No. 013192
DHA08401319207
Product Details
Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
M Ophthalmic devices
M1350 Keatoscope
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2023