"DGH" Keratoscope (Non-Sterile) - Taiwan Registration 2e9255a3eb34f53bfaacec3b50ddc3f5
Access comprehensive regulatory information for "DGH" 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 2e9255a3eb34f53bfaacec3b50ddc3f5 and manufactured by DGH Technology Inc.. 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 DGH Technology 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.
Device Details
Registration Details
2e9255a3eb34f53bfaacec3b50ddc3f5
Ministry of Health Medical Device Import Registration No. 017752
DHA08401775200
Product Details
M Ophthalmic devices
M1350 Keatoscope
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2022
Cancellation Information
Logged out
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