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"Fudona" Dinah Meis laser system - Taiwan Registration 21eb08b5f4ac53fdc24b0afc070fd07a

Access comprehensive regulatory information for "Fudona" Dinah Meis 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 21eb08b5f4ac53fdc24b0afc070fd07a 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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21eb08b5f4ac53fdc24b0afc070fd07a
Registration Details
Taiwan FDA Registration: 21eb08b5f4ac53fdc24b0afc070fd07a
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Device Details

"Fudona" Dinah Meis laser system
TW: โ€œๅฏŒๅคšๆ‹ฟโ€้ป›ๅจœ็พŽๆ–ฏ้›ทๅฐ„็ณป็ตฑ
Risk Class 2

Registration Details

21eb08b5f4ac53fdc24b0afc070fd07a

DHA00602504302

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

import

Dates and Status

May 25, 2013

May 25, 2028

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