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"AIMA" laser and pulsed illumination system - Taiwan Registration a5e9dcd478308dc26975b7ff38d5efd3

Access comprehensive regulatory information for "AIMA" laser and pulsed illumination system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a5e9dcd478308dc26975b7ff38d5efd3 and manufactured by Alma Lasers GmbH;; Alma Lasers Ltd.. The authorized representative in Taiwan is NEOASIA 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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a5e9dcd478308dc26975b7ff38d5efd3
Registration Details
Taiwan FDA Registration: a5e9dcd478308dc26975b7ff38d5efd3
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Device Details

"AIMA" laser and pulsed illumination system
TW: โ€œๆ„›็‘ชโ€้›ทๅฐ„ๅŠ่„ˆ่กๅ…‰็…ง็ณป็ตฑ
Risk Class 2

Registration Details

a5e9dcd478308dc26975b7ff38d5efd3

DHA00602243402

Company Information

Israel;;Germany

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 01, 2011

Jun 01, 2026