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"Nesi" stereoscope (unsterilized) - Taiwan Registration 5dbfd4a7a4592432f84d25537ab38330

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 5dbfd4a7a4592432f84d25537ab38330 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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5dbfd4a7a4592432f84d25537ab38330
Registration Details
Taiwan FDA Registration: 5dbfd4a7a4592432f84d25537ab38330
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Device Details

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

Registration Details

5dbfd4a7a4592432f84d25537ab38330

DHA04401182309

Company Information

Product Details

Limited to the first-level identification range of the medical equipment management measures "stereoscope (M.1870)".

M Ophthalmology

M.1870 Cubescope

import

Dates and Status

Jun 13, 2012

Jun 13, 2022

Sep 30, 2021

Cancellation Information

Logged out

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