"Nesi" stereoscope (unsterilized)
Taiwan·Risk Class 1·NEITZ INSTRUMENTS CO., LTD.·Registered Jun 13, 2012 – Jun 13, 2022Cancelled- Analysis ID
- 5dbfd4a7a4592432f84d25537ab38330
- Customs Code
- DHA04401182309
- Manufacturer
- NEITZ INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- BIOMEGA INSTRUMENT CO., LTD.
- Intended Use
- Limited to the first-level identification range of the medical equipment management measures "stereoscope (M.1870)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1870 Cubescope
- Import Information
- import
- Registration Date
- Jun 13, 2012
- Expiry Date
- Jun 13, 2022
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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.