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Niedek corneal radius measuring device - Taiwan Registration 9f95b1a4d78beb7e65461498ecf3b85f

Access comprehensive regulatory information for Niedek corneal radius measuring device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f95b1a4d78beb7e65461498ecf3b85f and manufactured by NIDEK CO., LTD.. The authorized representative in Taiwan is Emperor Prayer Limited.

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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9f95b1a4d78beb7e65461498ecf3b85f
Registration Details
Taiwan FDA Registration: 9f95b1a4d78beb7e65461498ecf3b85f
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Device Details

Niedek corneal radius measuring device
TW: ๅฐผๅพทๅ…‹่ง’่†œๅŠๅพ‘ๆธฌ้‡่ฃ็ฝฎ
Risk Class 1
Cancelled

Registration Details

9f95b1a4d78beb7e65461498ecf3b85f

DHA04400392801

Company Information

Japan

Product Details

It is limited to the first level of identification of the "Corneal Radius Measurement Device (M.1450)" of the Medical Device Management Regulations.

M Ophthalmology

M.1450 ่ง’่†œๅผงๅบฆ้‡ๆธฌๅ™จ

import

Dates and Status

Apr 15, 2006

Apr 15, 2011

Aug 11, 2006

Cancellation Information

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