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"E-Swin" Keratoscope (Non-Sterile) - Taiwan Registration 101931415e885c2221ced11dbcaf3d15

Access comprehensive regulatory information for "E-Swin" 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 101931415e885c2221ced11dbcaf3d15 and manufactured by E-SWIN. The authorized representative in Taiwan is CLINICO INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including E-SWIN, and 1 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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101931415e885c2221ced11dbcaf3d15
Registration Details
Taiwan FDA Registration: 101931415e885c2221ced11dbcaf3d15
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Device Details

"E-Swin" Keratoscope (Non-Sterile)
TW: "็›Š่ฆ–" ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

101931415e885c2221ced11dbcaf3d15

Ministry of Health Medical Device Import Registration No. 022176

DHA08402217600

Company Information

France

Product Details

Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026

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