Taiwan FDA registration 44daf2fdfdf2765fc83dc996eee14482

Le Fan Mask Light Therapy Instrument

TW: 樂迷亞面罩光療儀

Taiwan·Risk Class 2·Simon Technology Co., Ltd. Luzhu Factory·Registered Feb 15, 2017 – Feb 15, 2022Cancelled

Registration details

Analysis ID: 44daf2fdfdf2765fc83dc996eee14482

Company information

Manufacturer: Simon Technology Co., Ltd. Luzhu Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: YIAN HUNG 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: Contract manufacturing;; Domestic;; 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: Feb 15, 2017
Expiry Date: Feb 15, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Le Fan Mask Light Therapy Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 44daf2fdfdf2765fc83dc996eee14482 and manufactured by Simon Technology Co., Ltd. Luzhu Factory. The authorized representative in Taiwan is YIAN HUNG CO., LTD..

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