Taiwan FDA registration 56ae83ef8fc44309b28f8f5a8ba1be1e
"Retra" Miyan Q-switched neodymium Jacob laser system
TW: “雷特拉”媄妍Q開關釹雅各雷射系統
Taiwan·Risk Class 2·LTRA GLOBAL CO., LTD.·Registered Oct 05, 2020 – Oct 05, 2025ExpiredRegistration details
- Analysis ID
- 56ae83ef8fc44309b28f8f5a8ba1be1e
- Customs Code
- DHA05603399201
Company information
- Manufacturer
- LTRA GLOBAL CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- K2 INTERNATIONAL MEDICAL INC.
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
- Oct 05, 2020
- Expiry Date
- Oct 05, 2025
About this record
Access comprehensive regulatory information for "Retra" Miyan Q-switched neodymium Jacob 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 56ae83ef8fc44309b28f8f5a8ba1be1e and manufactured by LTRA GLOBAL CO., LTD.. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..
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