Taiwan FDA registration 600d26755d1af46994590815061c3b56

"Falma" Makkah Laser Pulse Therapy Device

TW: “法爾瑪”麥加瑪雷射脈衝治療儀

Taiwan·Risk Class 2·Formatk Systems Ltd.·Registered Sep 05, 2024 – Sep 05, 2029Active

Registration details

Analysis ID: 600d26755d1af46994590815061c3b56
Customs Code: DHA05603739108

Company information

Manufacturer: Formatk Systems Ltd.
Manufacturer Country: Israel
Authorized Representative: ABIO MEDICAL SYSTEM COPR.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4810 Lasers for general surgical, orthopaedic and dermatological use
Import Information: import

Dates and status

Registration Date: Sep 05, 2024
Expiry Date: Sep 05, 2029

About this record

Access comprehensive regulatory information for "Falma" Makkah Laser Pulse Therapy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 600d26755d1af46994590815061c3b56 and manufactured by Formatk Systems Ltd.. The authorized representative in Taiwan is ABIO MEDICAL SYSTEM COPR..

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