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"Lomenis" ophthalmic laser device - Taiwan Registration 1d474bca2b8ccc98a8d5c1148d58e843

Access comprehensive regulatory information for "Lomenis" ophthalmic laser device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d474bca2b8ccc98a8d5c1148d58e843 and manufactured by LUMENIS INC.. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM 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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1d474bca2b8ccc98a8d5c1148d58e843
Registration Details
Taiwan FDA Registration: 1d474bca2b8ccc98a8d5c1148d58e843
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Device Details

"Lomenis" ophthalmic laser device
TW: โ€œๆด›ๆ˜Žๅฐผๆ–ฏโ€็œผ็ง‘้›ทๅฐ„่ฃ็ฝฎ
Risk Class 2
Cancelled

Registration Details

1d474bca2b8ccc98a8d5c1148d58e843

DHA00601857008

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

Jan 30, 2008

Jan 30, 2013

Apr 24, 2015

Cancellation Information

Logged out

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