Taiwan FDA registration 19e50019eb9e655892d4b7157e2f8ee3

"SBM" Keratoscope (non-sterile)

TW: "斯伯恩" 角膜鏡 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SBM SISTEMI S.R.L.·Registered Oct 01, 2021 – Oct 31, 2024Expired
Registration details
Analysis ID
19e50019eb9e655892d4b7157e2f8ee3
License Form
Ministry of Health Medical Device Import Registration No. 020987
Customs Code
DHA08402098701
Company information
Manufacturer
SBM SISTEMI S.R.L.
Manufacturer Country
Italy
Authorized Representative
TAIWAN HWA IN ENTERPRISE CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1350 Keatoscope
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2024
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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 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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