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“Formatk” Alpha Laser and Intense Pulsed Light System - Taiwan Registration 65743121cf13f981f20caacb05b5da80

Access comprehensive regulatory information for “Formatk” Alpha Laser and Intense Pulsed Light System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 65743121cf13f981f20caacb05b5da80 and manufactured by Formatk Systems Ltd.. The authorized representative in Taiwan is ABIO MEDICAL SYSTEM COPR..

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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65743121cf13f981f20caacb05b5da80
Registration Details
Taiwan FDA Registration: 65743121cf13f981f20caacb05b5da80
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Device Details

“Formatk” Alpha Laser and Intense Pulsed Light System
TW: “法爾瑪”阿爾發雷射脈衝治療儀
Risk Class 2
MD

Registration Details

65743121cf13f981f20caacb05b5da80

Ministry of Health Medical Device Import No. 036500

DHA05603650008

Company Information

Israel

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

May 11, 2023

May 11, 2028