Taiwan FDA registration 0b165f0fb72115c532f758590b5fb19b
"Fudona" Levok laser system
TW: “富多拿”萊渥克雷射系統
Taiwan·Risk Class 2·Fotona d.o.o.·Registered Sep 19, 2012 – Sep 19, 2027ActiveRegistration details
- Analysis ID
- 0b165f0fb72115c532f758590b5fb19b
- Customs Code
- DHA00602403501
Company information
- Manufacturer
- Fotona d.o.o.
- Manufacturer Country
- Slovenia
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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
- import
Dates and status
- Registration Date
- Sep 19, 2012
- Expiry Date
- Sep 19, 2027
About this record
Access comprehensive regulatory information for "Fudona" Levok 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 0b165f0fb72115c532f758590b5fb19b and manufactured by Fotona d.o.o.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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.
Free DatabasePowered by Pure Global AI89,000+ Devices