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"Nesi" stereoscope (unsterilized) - Taiwan Registration 861320d1570d0f375da6cb616c9aa917

Access comprehensive regulatory information for "Nesi" stereoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 861320d1570d0f375da6cb616c9aa917 and manufactured by NEITZ INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT 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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861320d1570d0f375da6cb616c9aa917
Registration Details
Taiwan FDA Registration: 861320d1570d0f375da6cb616c9aa917
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Device Details

"Nesi" stereoscope (unsterilized)
TW: โ€œ่€ๅธโ€็ซ‹้ซ”้ก(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

861320d1570d0f375da6cb616c9aa917

DHA08401182306

Company Information

Product Details

It is limited to the first-level identification scope of the "Stereoscope (M.1870)" Administrative Measures for the Classification and Grading of Medical Devices.

M Ophthalmology

M.1870 Cubescope

import

Dates and Status

Oct 01, 2021

Oct 31, 2025

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