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Revision Overnight Wear Orthokeratology Contact Lens - Taiwan Registration 5ea5bf1d60a6e45670f2b1805f8befae

Access comprehensive regulatory information for Revision Overnight Wear Orthokeratology Contact Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5ea5bf1d60a6e45670f2b1805f8befae and manufactured by Eagle Vision Co., Ltd. Shilin Factory. The authorized representative in Taiwan is VISION TECHNOLOGY 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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5ea5bf1d60a6e45670f2b1805f8befae
Registration Details
Taiwan FDA Registration: 5ea5bf1d60a6e45670f2b1805f8befae
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Device Details

Revision Overnight Wear Orthokeratology Contact Lens
TW: ้Šณ่ฆ–ๅคœๆˆดๅž‹่ง’่†œๅก‘ๅž‹้šฑๅฝข็œผ้ก
Risk Class 3
MD

Registration Details

5ea5bf1d60a6e45670f2b1805f8befae

Ministry of Health Medical Device Manufacturing No. 006792

Company Information

Taiwan, Province of China

Product Details

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

M Ophthalmic devices

M5916 Rigid breathable contact lens

Produced in Taiwan, China

Dates and Status

May 14, 2020

Dec 19, 2027