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"Fudona" Max Neodymium Jacques laser system - Taiwan Registration eb811cca9511305cabd1ae4a40553f23

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..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Fotona d.o.o., and 1 recent registrations in the same category. 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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eb811cca9511305cabd1ae4a40553f23
Registration Details
Taiwan FDA Registration: eb811cca9511305cabd1ae4a40553f23
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Device Details

"Fudona" Max Neodymium Jacques laser system
TW: โ€œๅฏŒๅคšๆ‹ฟโ€้บฅๅ…‹ๆ–ฏ้‡น้›…ๅ…‹้›ทๅฐ„็ณป็ตฑ
Risk Class 2

Registration Details

eb811cca9511305cabd1ae4a40553f23

DHA05602868702

Company Information

Slovenia

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

Jul 13, 2016

Jul 13, 2026

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