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"NIDEK" Tabletop Refraction System (Non-Sterile) - Taiwan Registration bbb940e706a9243c60e2d47c124c98fa

Access comprehensive regulatory information for "NIDEK" Tabletop Refraction System (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 bbb940e706a9243c60e2d47c124c98fa and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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bbb940e706a9243c60e2d47c124c98fa
Registration Details
Taiwan FDA Registration: bbb940e706a9243c60e2d47c124c98fa
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Device Details

"NIDEK" Tabletop Refraction System (Non-Sterile)
TW: "ๅฐผๅพทๅ…‹"ๆกŒไธŠๅž‹ๅฑˆๅ…‰็ณป็ตฑ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

bbb940e706a9243c60e2d47c124c98fa

Ministry of Health Medical Device Import No. 018401

DHA09401840101

Company Information

Product Details

M Ophthalmic devices

M1760 Ophthalmic Refractive Machine

Imported from abroad

Dates and Status

Oct 13, 2017

Oct 13, 2022

Cancellation Information

Logged out

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