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"Cooldra" Inleiden three-picosecond laser system and accessories - Taiwan Registration 2868b79b48a2187dd4405c5745a27e6d

Access comprehensive regulatory information for "Cooldra" Inleiden three-picosecond laser system and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2868b79b48a2187dd4405c5745a27e6d and manufactured by CUTERA, INC.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL 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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2868b79b48a2187dd4405c5745a27e6d
Registration Details
Taiwan FDA Registration: 2868b79b48a2187dd4405c5745a27e6d
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Device Details

"Cooldra" Inleiden three-picosecond laser system and accessories
TW: โ€œ้…ทๅพทๆ‹‰โ€ๅ› ่Š้ “ๅ็šฎ็ง’้›ทๅฐ„็ณป็ตฑๅŠๅ…ถ้…ไปถ
Risk Class 2

Registration Details

2868b79b48a2187dd4405c5745a27e6d

DHA05603094503

Company Information

United States

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

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". input

Dates and Status

Mar 05, 2018

Mar 05, 2028