Taiwan FDA registration 4376a9b736cd6dd878162d769e896009
"Meiqiang" laser therapy device
TW: "美強"雷射治療器
Taiwan·Risk Class 2·METRON MEDICAL AUSTRALIA PTY LTD.·Registered Apr 13, 2005 – Apr 13, 2020CancelledRegistration details
- Analysis ID
- 4376a9b736cd6dd878162d769e896009
- Customs Code
- DHA00601117802
Company information
- Manufacturer
- METRON MEDICAL AUSTRALIA PTY LTD.
- Manufacturer Country
- Australia
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS 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
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 2005
- Expiry Date
- Apr 13, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Meiqiang" laser therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4376a9b736cd6dd878162d769e896009 and manufactured by METRON MEDICAL AUSTRALIA PTY LTD.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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