Taiwan FDA registration 9e09ab09b9acf841fab257e1316d60c4
Optos ophthalmic rubidium chromium laser
TW: 澳普拓思眼科銣雅鉻雷射
Registration details
- Analysis ID
- 9e09ab09b9acf841fab257e1316d60c4
- Customs Code
- DHY00500347505
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
- Oct 24, 2011
- Expiry Date
- Nov 27, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Optos ophthalmic rubidium chromium laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e09ab09b9acf841fab257e1316d60c4 and manufactured by LIGHTMED CORPORATION. The authorized representative in Taiwan is LIGHTMED CORPORATION.
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