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"NEITZ" Keratoscope (Non-Sterile) - Taiwan Registration f5f239a6819b72e1cc0bfec0c80ab707

Access comprehensive regulatory information for "NEITZ" 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 f5f239a6819b72e1cc0bfec0c80ab707 and manufactured by NEITZ INSTRUMENTS CO., LTD.. 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 NEITZ INSTRUMENTS CO., LTD., 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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f5f239a6819b72e1cc0bfec0c80ab707
Registration Details
Taiwan FDA Registration: f5f239a6819b72e1cc0bfec0c80ab707
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Device Details

"NEITZ" Keratoscope (Non-Sterile)
TW: "่€ๆ–ฏ"่ง’่†œ้ก(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

f5f239a6819b72e1cc0bfec0c80ab707

Ministry of Health Medical Device Import No. 020318

DHA09402031803

Company Information

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Apr 16, 2019

Apr 16, 2024

Cancellation Information

Logged out

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