Taiwan FDA registration fc0db080ed505bf4c9f04ddf98229b75
Leonardo Dual Laser System
TW: 李奧納多雙頻雷射儀
Taiwan·Risk Class 2·MD·CeramOptec GmbH·Registered Dec 10, 2018 – Dec 10, 2023ExpiredRegistration details
- Analysis ID
- fc0db080ed505bf4c9f04ddf98229b75
- License Form
- Ministry of Health Medical Device Import No. 031921
- Customs Code
- DHA05603192107
Company information
- Manufacturer
- CeramOptec GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- ANDERSON MEDICAL SUPPLY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 10, 2018
- Expiry Date
- Dec 10, 2023
About this record
Access comprehensive regulatory information for Leonardo Dual 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 fc0db080ed505bf4c9f04ddf98229b75 and manufactured by CeramOptec GmbH. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY CO., LTD..
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