Taiwan FDA registration e038c03722db2f232e802066e81b95c4
Leonardo Laser System
TW: 李奧納多雷射儀
Taiwan·Risk Class 2·MD·CeramOptec GmbH·Registered Apr 17, 2017 – Apr 17, 2027ActiveRegistration details
- Analysis ID
- e038c03722db2f232e802066e81b95c4
- License Form
- Ministry of Health Medical Device Import No. 029635
- Customs Code
- DHA05602963501
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
- Apr 17, 2017
- Expiry Date
- Apr 17, 2027
About this record
Access comprehensive regulatory information for Leonardo 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 e038c03722db2f232e802066e81b95c4 and manufactured by CeramOptec GmbH. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY 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