"NEITZ" Keratoscope (Non-Sterile) - Taiwan Registration 7e411cf4711b855067cd1d080bda22a3
Access comprehensive regulatory information for "NEITZ" Keratoscope (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 7e411cf4711b855067cd1d080bda22a3 and manufactured by NEITZ INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NEITZ INSTRUMENTS 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
7e411cf4711b855067cd1d080bda22a3
Ministry of Health Medical Device Import Registration No. 020318
DHA08402031807
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, 2024

