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Aimei Contact Lens Eye Relief Solution - Taiwan Registration 9bdfdf78deaf0e380e06d7e2efc5d0e1

Access comprehensive regulatory information for Aimei Contact Lens Eye Relief Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9bdfdf78deaf0e380e06d7e2efc5d0e1 and manufactured by AVIZOR S.A.. The authorized representative in Taiwan is JI CHANG ENTERPRISE CO..

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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9bdfdf78deaf0e380e06d7e2efc5d0e1
Registration Details
Taiwan FDA Registration: 9bdfdf78deaf0e380e06d7e2efc5d0e1
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Device Details

Aimei Contact Lens Eye Relief Solution
TW: ๆ„›็พŽ่ฆ–้šฑๅฝข็œผ้ก่ˆ’็œผๆถฒ
Risk Class 2
Cancelled

Registration Details

9bdfdf78deaf0e380e06d7e2efc5d0e1

DHA00602421806

Company Information

Spain

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.5928 Products for the preservation of soft contact lenses

import

Dates and Status

Dec 04, 2012

Dec 04, 2022

Apr 12, 2024

Cancellation Information

Logged out

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