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"APRAMED" Keratoscope (Non-Sterile) - Taiwan Registration de21213d988e7caf6f2389feade2be89

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 de21213d988e7caf6f2389feade2be89 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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de21213d988e7caf6f2389feade2be89
Registration Details
Taiwan FDA Registration: de21213d988e7caf6f2389feade2be89
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Device Details

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

Registration Details

de21213d988e7caf6f2389feade2be89

Ministry of Health Medical Device Import Registration No. 018390

DHA08401839000

Company Information

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, 2023

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