"SBM" Keratoscope (non-sterile) - Taiwan Registration 19e50019eb9e655892d4b7157e2f8ee3
Access comprehensive regulatory information for "SBM" 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 19e50019eb9e655892d4b7157e2f8ee3 and manufactured by SBM SISTEMI S.R.L.. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SBM SISTEMI S.R.L., SBM SISTEMI, and 3 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
19e50019eb9e655892d4b7157e2f8ee3
Ministry of Health Medical Device Import Registration No. 020987
DHA08402098701
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
"SBM" Keratoscope (non-sterile)
SBM SISTEMI S.R.L.
e3865eda6bf6ec9897f2e5ce97f6151a
1
"SBM" Keratoscope (Non-Sterile)
SBM SISTEMI
86d56ea12acc1eeec3286f9570240ea5
1
"SBM" Keratoscope (Non-Sterile)
SBM SISTEMI S.R.L.
917bdc7b448d41f8cdcf2d91f8262151
1

