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"Lominnis" Viyi eye laser system - Taiwan Registration fd6f8aaaa7b004c7783543b8b1d6821c

Access comprehensive regulatory information for "Lominnis" Viyi eye laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd6f8aaaa7b004c7783543b8b1d6821c and manufactured by LUMENIS INC.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.

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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fd6f8aaaa7b004c7783543b8b1d6821c
Registration Details
Taiwan FDA Registration: fd6f8aaaa7b004c7783543b8b1d6821c
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Device Details

"Lominnis" Viyi eye laser system
TW: โ€œๆด›ๆ˜Žๅฐผๆ–ฏโ€็ถญไพ็œผ็”จ้›ทๅฐ„็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

fd6f8aaaa7b004c7783543b8b1d6821c

DHA00602418606

Company Information

United States

Product Details

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

M Ophthalmology

M.4390 ็œผ็ง‘้›ทๅฐ„่ฃ็ฝฎ

import

Dates and Status

Nov 07, 2012

Nov 07, 2022

Apr 12, 2024

Cancellation Information

Logged out

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