Taiwan FDA registration 05b31f78fcb2fcd65d01ebc2097cfaeb
"Chengxian" multi-wavelength medical laser therapy instrument
TW: “承賢”多波長醫用雷射治療儀
Taiwan·Risk Class 2·LIGHTMED CORPORATION·Registered Nov 27, 2012 – Nov 27, 2017CancelledRegistration details
- Analysis ID
- 05b31f78fcb2fcd65d01ebc2097cfaeb
Company information
- Manufacturer
- LIGHTMED CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LIGHTMED CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4390 眼科雷射裝置
- Import Information
- Domestic
Dates and status
- Registration Date
- Nov 27, 2012
- Expiry Date
- Nov 27, 2017
- Cancellation Date
- Nov 26, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Chengxian" multi-wavelength medical 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 05b31f78fcb2fcd65d01ebc2097cfaeb and manufactured by LIGHTMED CORPORATION. The authorized representative in Taiwan is LIGHTMED CORPORATION.
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