Pure Global

“ALMA” Harmony XL PRO System - Taiwan Registration c246e2b7f3459476886001f99d83f4d8

Access comprehensive regulatory information for “ALMA” Harmony XL PRO System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c246e2b7f3459476886001f99d83f4d8 and manufactured by 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
c246e2b7f3459476886001f99d83f4d8
Registration Details
Taiwan FDA Registration: c246e2b7f3459476886001f99d83f4d8
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“ALMA” Harmony XL PRO System
TW: “愛瑪”瀚墨霓雷射光電系統
Risk Class 2
MD

Registration Details

c246e2b7f3459476886001f99d83f4d8

Ministry of Health Medical Device Import No. 030043

DHA05603004302

Company Information

Israel

Product Details

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

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad; Contract manufacturing;; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"

Dates and Status

Aug 03, 2017

Aug 03, 2027