Taiwan FDA registration 9be77cf94f645400f84ac8b7b72ffb30

"Cuitra" Alice Chrome laser system and accessories thereof

TW: “奎特拉”愛麗絲雅鉻雷射系統及其配件

Taiwan·Risk Class 2·CUTERA, INC.·Registered Mar 05, 2018 – Mar 05, 2028Active

Registration details

Analysis ID: 9be77cf94f645400f84ac8b7b72ffb30
Customs Code: DHA05603093806

Company information

Manufacturer: CUTERA, INC.
Manufacturer Country: United States
Authorized Representative: AESOLUTION BIOMEDICAL CO. LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
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: Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and status

Registration Date: Mar 05, 2018
Expiry Date: Mar 05, 2028

About this record

Access comprehensive regulatory information for "Cuitra" Alice Chrome laser system and accessories thereof in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9be77cf94f645400f84ac8b7b72ffb30 and manufactured by CUTERA, INC.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..

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