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"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.

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19e50019eb9e655892d4b7157e2f8ee3
Registration Details
Taiwan FDA Registration: 19e50019eb9e655892d4b7157e2f8ee3
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Device Details

"SBM" Keratoscope (non-sterile)
TW: "ๆ–ฏไผฏๆฉ" ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

19e50019eb9e655892d4b7157e2f8ee3

Ministry of Health Medical Device Import Registration No. 020987

DHA08402098701

Company Information

Italy

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

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