Taiwan FDA registration 75d74a1f553497d4e26709cfc41c1fdf
Opto ophthalmic rubidium chromium laser
TW: 澳普拓眼科銣雅鉻雷射
Taiwan·Risk Class 2·LIGHTMED CORPORATION·Registered Apr 02, 2007 – Nov 27, 2015CancelledRegistration details
- Analysis ID
- 75d74a1f553497d4e26709cfc41c1fdf
- Customs Code
- DHY00500215600
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.4392 後囊切除用Nd:YAG雷射
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 02, 2007
- 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 Opto 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 75d74a1f553497d4e26709cfc41c1fdf and manufactured by LIGHTMED CORPORATION. The authorized representative in Taiwan is LIGHTMED CORPORATION.
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