Taiwan FDA registration e3865eda6bf6ec9897f2e5ce97f6151a

"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 28, 2019 – Oct 28, 2024Cancelled
Registration details
Analysis ID
e3865eda6bf6ec9897f2e5ce97f6151a
License Form
Ministry of Health Medical Device Import No. 020987
Customs Code
DHA09402098707
Company information
Manufacturer
SBM SISTEMI S.R.L.
Manufacturer Country
Italy
Authorized Representative
TAIWAN HWA IN ENTERPRISE CO., LTD.
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
Oct 28, 2019
Expiry Date
Oct 28, 2024
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 e3865eda6bf6ec9897f2e5ce97f6151a 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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