"APRAMED" Keratoscope (Non-Sterile) - Taiwan Registration de21213d988e7caf6f2389feade2be89
Access comprehensive regulatory information for "APRAMED" 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 de21213d988e7caf6f2389feade2be89 and manufactured by APRAMED IND E COM DE APARELHOS MEDICOS LTDA. 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 APRAMED IND E COM DE APARELHOS MEDICOS LTDA, 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
de21213d988e7caf6f2389feade2be89
Ministry of Health Medical Device Import Registration No. 018390
DHA08401839000
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

