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Le Fan Mask Light Therapy Instrument - Taiwan Registration 44daf2fdfdf2765fc83dc996eee14482

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..

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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44daf2fdfdf2765fc83dc996eee14482
Registration Details
Taiwan FDA Registration: 44daf2fdfdf2765fc83dc996eee14482
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Device Details

Le Fan Mask Light Therapy Instrument
TW: ๆจ‚่ฟทไบž้ข็ฝฉๅ…‰็™‚ๅ„€
Risk Class 2
Cancelled

Registration Details

44daf2fdfdf2765fc83dc996eee14482

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

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

Feb 15, 2017

Feb 15, 2022

Apr 12, 2024

Cancellation Information

Logged out

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