Taiwan FDA registration 3c82e92a686855b04c6f519a3a30f679
"Photon" laser therapy instrument
TW: “光子”雷射治療儀
Taiwan·Risk Class 2·BIOPHOTON SA·Registered Oct 03, 2005 – Oct 03, 2015CancelledRegistration details
- Analysis ID
- 3c82e92a686855b04c6f519a3a30f679
- Customs Code
- DHA00601312300
Company information
- Manufacturer
- BIOPHOTON SA
- Manufacturer Country
- France
- Authorized Representative
- CROWNMED ENTERPRISE 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
Dates and status
- Registration Date
- Oct 03, 2005
- Expiry Date
- Oct 03, 2015
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Photon" laser therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3c82e92a686855b04c6f519a3a30f679 and manufactured by BIOPHOTON SA. The authorized representative in Taiwan is CROWNMED ENTERPRISE CO., LTD..
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