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"MEDMONT" Keratoscope(Non-Sterile) - Taiwan Registration 5517bdbd9041208c5cad76a669d249ea

Access comprehensive regulatory information for "MEDMONT" 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 5517bdbd9041208c5cad76a669d249ea and manufactured by MEDMONT INTERNATIONAL PTY LTD. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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5517bdbd9041208c5cad76a669d249ea
Registration Details
Taiwan FDA Registration: 5517bdbd9041208c5cad76a669d249ea
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Device Details

"MEDMONT" Keratoscope(Non-Sterile)
TW: "็พŽ่†œ" ่ง’่†œ้ก(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5517bdbd9041208c5cad76a669d249ea

Ministry of Health Medical Device Import Registration No. 010462

DHA08401046208

Company Information

Australia

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