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"Lominnis" pulsed illumination / rubidium Yak / diode laser system - Taiwan Registration f8a9b5d2f931c6b933f6ff5625218d30

Access comprehensive regulatory information for "Lominnis" pulsed illumination / rubidium Yak / diode 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 f8a9b5d2f931c6b933f6ff5625218d30 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is LUMENIS (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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f8a9b5d2f931c6b933f6ff5625218d30
Registration Details
Taiwan FDA Registration: f8a9b5d2f931c6b933f6ff5625218d30
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Device Details

"Lominnis" pulsed illumination / rubidium Yak / diode laser system
TW: โ€œๆด›ๆ˜Žๅฐผๆ–ฏโ€่„ˆ่กๅผๅ…‰็…ง/ ้Šฃ้›…ๅ…‹/ ไบŒๆฅต้ซ”้›ทๅฐ„็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

f8a9b5d2f931c6b933f6ff5625218d30

DHA00601888303

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

Jun 02, 2008

Jun 02, 2018

Dec 13, 2019

Cancellation Information

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