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"Lomenis" pulsed light/laser and its accessories - Taiwan Registration a6008231fcecc50d59fc6ccd861c961c

Access comprehensive regulatory information for "Lomenis" 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 a6008231fcecc50d59fc6ccd861c961c and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is MOSTYLE CORPORATION.

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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a6008231fcecc50d59fc6ccd861c961c
Registration Details
Taiwan FDA Registration: a6008231fcecc50d59fc6ccd861c961c
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Device Details

"Lomenis" pulsed light/laser and its accessories
TW: "ๆด›ๆ˜Žๅฐผๆ–ฏ"่„ˆ่กๅ…‰/้›ทๅฐ„ๅ„€ๅŠๅ…ถ้…ไปถ
Risk Class 2
Cancelled

Registration Details

a6008231fcecc50d59fc6ccd861c961c

DHA00601702902

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

Aug 23, 2006

Aug 23, 2011

Nov 27, 2012

Cancellation Information

Logged out

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