Taiwan FDA registration eb811cca9511305cabd1ae4a40553f23

"Fudona" Max Neodymium Jacques laser system

TW: “富多拿”麥克斯釹雅克雷射系統
Taiwan flagTaiwan·Risk Class 2·Fotona d.o.o.·Registered Jul 13, 2016 – Jul 13, 2026Expired
Registration details
Analysis ID
eb811cca9511305cabd1ae4a40553f23
Customs Code
DHA05602868702
Company information
Manufacturer
Fotona d.o.o.
Manufacturer Country
Slovenia
Authorized Representative
DYNAMIC MEDICAL TECHNOLOGIES INC.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4810 Lasers for general surgical, orthopaedic and dermatological use
Import Information
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
Registration Date
Jul 13, 2016
Expiry Date
Jul 13, 2026
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About this record

Access comprehensive regulatory information for "Fudona" Max Neodymium Jacques 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 eb811cca9511305cabd1ae4a40553f23 and manufactured by Fotona d.o.o.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

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