Pure Global

"Cuitra" Alice Chrome laser system and accessories thereof - Taiwan Registration 9be77cf94f645400f84ac8b7b72ffb30

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..

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
9be77cf94f645400f84ac8b7b72ffb30
Registration Details
Taiwan FDA Registration: 9be77cf94f645400f84ac8b7b72ffb30
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Cuitra" Alice Chrome laser system and accessories thereof
TW: โ€œๅฅŽ็‰นๆ‹‰โ€ๆ„›้บ—็ตฒ้›…้‰ป้›ทๅฐ„็ณป็ตฑๅŠๅ…ถ้…ไปถ
Risk Class 2

Registration Details

9be77cf94f645400f84ac8b7b72ffb30

DHA05603093806

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

Mar 05, 2018

Mar 05, 2028