Taiwan FDA registration f6cdbd09078226b913bc28be96d97d3d
"Capital" Q-switched neodymium Jacob laser
TW: “首都”Q開關釹雅各雷射儀
Taiwan·Risk Class 2·SOODO GROUP·Registered Aug 31, 2012 – Aug 31, 2017CancelledRegistration details
- Analysis ID
- f6cdbd09078226b913bc28be96d97d3d
- Customs Code
- DHA00602390000
Company information
- Manufacturer
- SOODO GROUP
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MARIAN BIOMEDICAL TECHNOLOGY CO., LTD.
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
- Aug 31, 2012
- Expiry Date
- Aug 31, 2017
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Capital" Q-switched neodymium Jacob laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f6cdbd09078226b913bc28be96d97d3d and manufactured by SOODO GROUP. The authorized representative in Taiwan is MARIAN BIOMEDICAL TECHNOLOGY 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