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"SBM" Keratoscope (Non-Sterile) - Taiwan Registration 86d56ea12acc1eeec3286f9570240ea5

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 86d56ea12acc1eeec3286f9570240ea5 and manufactured by SBM SISTEMI. The authorized representative in Taiwan is CLINICO INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SBM SISTEMI S.R.L., 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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86d56ea12acc1eeec3286f9570240ea5
Registration Details
Taiwan FDA Registration: 86d56ea12acc1eeec3286f9570240ea5
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Device Details

"SBM" Keratoscope (Non-Sterile)
TW: "่ฆ–ๅฟ…็พŽ" ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

86d56ea12acc1eeec3286f9570240ea5

Ministry of Health Medical Device Import No. 018925

DHA09401892506

Company Information

Italy

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Mar 23, 2018

Mar 23, 2023

Cancellation Information

Logged out

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