"Kendela" Flying Shuttle laser system - Taiwan Registration 5524f67ea2fb66aedefe8ea0a9db6d82
Access comprehensive regulatory information for "Kendela" Flying Shuttle laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5524f67ea2fb66aedefe8ea0a9db6d82 and manufactured by NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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.
Device Details
Registration Details
5524f67ea2fb66aedefe8ea0a9db6d82
DHA05603165907
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;; Contract manufacturing;; 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
Aug 21, 2023
Oct 02, 2028