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"APRAMED" Keratoscope (Non-Sterile) - Taiwan Registration f75d6afa3b47d63d4d4d3a069d20d843

Access comprehensive regulatory information for "APRAMED" 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 f75d6afa3b47d63d4d4d3a069d20d843 and manufactured by APRAMED IND E COM DE APARELHOS MEDICOS LTDA. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including APRAMED IND E COM DE APARELHOS MEDICOS LTDA, 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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f75d6afa3b47d63d4d4d3a069d20d843
Registration Details
Taiwan FDA Registration: f75d6afa3b47d63d4d4d3a069d20d843
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Device Details

"APRAMED" Keratoscope (Non-Sterile)
TW: "้˜ฟๆฒ›่ˆ็พŽ" ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

f75d6afa3b47d63d4d4d3a069d20d843

Ministry of Health Medical Device Import No. 018390

DHA09401839006

Company Information

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Oct 11, 2017

Oct 11, 2022

Cancellation Information

Logged out

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