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“Sharplight” Omnimax System - Taiwan Registration c61ecdf7be94d72a085ba83dacd73724

Access comprehensive regulatory information for “Sharplight” Omnimax System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c61ecdf7be94d72a085ba83dacd73724 and manufactured by SharpLight Technologies Ltd.. The authorized representative in Taiwan is COLLAMATRIX CO., 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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c61ecdf7be94d72a085ba83dacd73724
Registration Details
Taiwan FDA Registration: c61ecdf7be94d72a085ba83dacd73724
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Device Details

“Sharplight” Omnimax System
TW: “夏普萊特”歐尼美系統
Risk Class 2
MD

Registration Details

c61ecdf7be94d72a085ba83dacd73724

Ministry of Health Medical Device Import No. 031583

DHA05603158300

Company Information

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

Dates and Status

Sep 03, 2018

Sep 03, 2023