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"Kudra" Inleidensl picosecond laser system and its accessories - Taiwan Registration 89b7d6f2b25d8b9cdde18eac9278ac05

Access comprehensive regulatory information for "Kudra" Inleidensl picosecond laser system and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 89b7d6f2b25d8b9cdde18eac9278ac05 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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89b7d6f2b25d8b9cdde18eac9278ac05
Registration Details
Taiwan FDA Registration: 89b7d6f2b25d8b9cdde18eac9278ac05
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Device Details

"Kudra" Inleidensl picosecond laser system and its accessories
TW: โ€œ้…ทๅพทๆ‹‰โ€ๅ› ่Š้ “ๆ–ฏ็ˆพ็šฎ็ง’้›ทๅฐ„็ณป็ตฑๅŠๅ…ถ้…ไปถ
Risk Class 2

Registration Details

89b7d6f2b25d8b9cdde18eac9278ac05

DHA05603166502

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

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

Oct 08, 2018

Oct 08, 2028