Taiwan FDA registration f550e85d546b109c7dfb3e992eb0004d
“LEONI” Laser Fiber
TW: “雷奧尼”雷射光纖
Taiwan·Risk Class 2·MD·LEONI Fiber Optics, Inc.·Registered Dec 13, 2022 – Dec 13, 2027ActiveRegistration details
- Analysis ID
- f550e85d546b109c7dfb3e992eb0004d
- License Form
- Ministry of Health Medical Device Import No. 036128
- Customs Code
- DHA05603612801
Company information
- Manufacturer
- LEONI Fiber Optics, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- SMARTECH MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 13, 2022
- Expiry Date
- Dec 13, 2027
About this record
Access comprehensive regulatory information for “LEONI” Laser Fiber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f550e85d546b109c7dfb3e992eb0004d and manufactured by LEONI Fiber Optics, Inc.. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..
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