Taiwan FDA registration 861320d1570d0f375da6cb616c9aa917

"Nesi" stereoscope (unsterilized)

TW: “耐司”立體鏡(未滅菌)
Taiwan flagTaiwan·Risk Class 1·NEITZ INSTRUMENTS CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
861320d1570d0f375da6cb616c9aa917
Customs Code
DHA08401182306
Company information
Manufacturer Country
Japan
Authorized Representative
BIOMEGA INSTRUMENT CO., LTD.
Product details
Intended Use
It is limited to the first-level identification scope of the "Stereoscope (M.1870)" Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.1870 Cubescope
Import Information
import
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

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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