"Fudona" Max Neodymium Jacques laser system
- Analysis ID
- eb811cca9511305cabd1ae4a40553f23
- Customs Code
- DHA05602868702
- Manufacturer
- Fotona d.o.o.
- Manufacturer Country
- Slovenia
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
- 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
- Registration Date
- Jul 13, 2016
- Expiry Date
- Jul 13, 2026
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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.