Taiwan FDA registration ae1e0ddbfac01674df5363b61ead3366
"Seunghyun" ophthalmic dual-wavelength laser treatment instrument
TW: “承賢”眼科雙波長雷射治療儀
Taiwan·Risk Class 2·LIGHTMED CORPORATION·Registered Mar 24, 2010 – Mar 24, 2030ActiveRegistration details
- Analysis ID
- ae1e0ddbfac01674df5363b61ead3366
- Customs Code
- DHY00500291005
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
- Mar 24, 2010
- Expiry Date
- Mar 24, 2030
About this record
Access comprehensive regulatory information for "Seunghyun" ophthalmic dual-wavelength laser treatment instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae1e0ddbfac01674df5363b61ead3366 and manufactured by LIGHTMED CORPORATION. The authorized representative in Taiwan is LIGHTMED CORPORATION.
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