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"NEITZ" Keratoscope (Non-Sterile) - Taiwan Registration 7e411cf4711b855067cd1d080bda22a3

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 7e411cf4711b855067cd1d080bda22a3 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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7e411cf4711b855067cd1d080bda22a3
Registration Details
Taiwan FDA Registration: 7e411cf4711b855067cd1d080bda22a3
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Device Details

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

Registration Details

7e411cf4711b855067cd1d080bda22a3

Ministry of Health Medical Device Import Registration No. 020318

DHA08402031807

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, 2024

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