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"Lominnis" Celite glaucoma laser - Taiwan Registration e776d468e2bcd934d0bcb99e591ea6a9

Access comprehensive regulatory information for "Lominnis" Celite glaucoma laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e776d468e2bcd934d0bcb99e591ea6a9 and manufactured by LUMENIS, INC.. The authorized representative in Taiwan is Taiwan Branch of Hong Kong Commercial Medical Laser 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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e776d468e2bcd934d0bcb99e591ea6a9
Registration Details
Taiwan FDA Registration: e776d468e2bcd934d0bcb99e591ea6a9
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Device Details

"Lominnis" Celite glaucoma laser
TW: โ€œๆด›ๆ˜Žๅฐผๆ–ฏโ€่‰ฒ้บ—็‰น้’ๅ…‰็œผ้›ทๅฐ„ๅ„€
Risk Class 2
Cancelled

Registration Details

e776d468e2bcd934d0bcb99e591ea6a9

DHA00602007200

Company Information

United States

Product Details

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

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

import

Dates and Status

Jul 21, 2009

Jul 21, 2014

Apr 25, 2018

Cancellation Information

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