Taiwan FDA registration 917bdc7b448d41f8cdcf2d91f8262151

"SBM" Keratoscope (Non-Sterile)

TW: "視比美" 角膜鏡 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SBM SISTEMI S.R.L.·Registered Dec 04, 2017 – Dec 04, 2022Cancelled
Registration details
Analysis ID
917bdc7b448d41f8cdcf2d91f8262151
License Form
Ministry of Health Medical Device Import No. 018568
Customs Code
DHA09401856808
Company information
Manufacturer
SBM SISTEMI S.R.L.
Manufacturer Country
Italy
Authorized Representative
EVERVISION INSTRUMENT CO.
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1350 Keatoscope
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 04, 2017
Expiry Date
Dec 04, 2022
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

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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