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"SBM" Keratoscope (Non-Sterile) - Taiwan Registration 917bdc7b448d41f8cdcf2d91f8262151

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 917bdc7b448d41f8cdcf2d91f8262151 and manufactured by SBM SISTEMI S.R.L.. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..

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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917bdc7b448d41f8cdcf2d91f8262151
Registration Details
Taiwan FDA Registration: 917bdc7b448d41f8cdcf2d91f8262151
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Device Details

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

Registration Details

917bdc7b448d41f8cdcf2d91f8262151

Ministry of Health Medical Device Import No. 018568

DHA09401856808

Company Information

Italy

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Dec 04, 2017

Dec 04, 2022

Cancellation Information

Logged out

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