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"Lominnis" lightteng pulsed light / laser and its accessories - Taiwan Registration ef6a4f7bfa5d6d33a2d3611ab2e21bc6

Access comprehensive regulatory information for "Lominnis" lightteng pulsed light / laser and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ef6a4f7bfa5d6d33a2d3611ab2e21bc6 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is LUMENIS (HK) LIMITED TAIWAN BRANCH.

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ef6a4f7bfa5d6d33a2d3611ab2e21bc6
Registration Details
Taiwan FDA Registration: ef6a4f7bfa5d6d33a2d3611ab2e21bc6
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Device Details

"Lominnis" lightteng pulsed light / laser and its accessories
TW: โ€œๆด›ๆ˜Žๅฐผๆ–ฏโ€ๅ…‰้จฐ่„ˆ่กๅ…‰/ ้›ทๅฐ„ๅ„€ๅŠๅ…ถ้…ไปถ
Risk Class 2
Cancelled

Registration Details

ef6a4f7bfa5d6d33a2d3611ab2e21bc6

DHA00601956405

Company Information

Israel

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

Jan 16, 2009

Jan 16, 2019

May 19, 2022

Cancellation Information

Logged out

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